Part B: Supplementary Information Sheet (SIS) |
FR Recognition List Number
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059
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Date of Entry 12/19/2022
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FR Recognition Number
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1-157
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Standard | |
ISO 10079-1 Fourth edition 2022-03 Medical suction equipment - Part 1: Electrically powered suction equipment |
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Scope/AbstractThis document specifies safety and performance requirements for electrically powered medical and surgical suction equipment. It applies to equipment used in health care facilities such as hospitals, for domiciliary care of patients and for field use and transport use. |
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Extent of Recognition
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Rationale for Recognition
This standard is relevant to medical devices and is recognized because it is scientifically and technically valid and not in conflict with existing regulatory policies. |
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Public Law, CFR Citation(s) and Procode(s)*
Regulation Number |
Device Name |
Device Class |
Product Code |
§870.5050 |
Apparatus, Suction, Patient Care
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Class 2
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DWM
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§870.5910 |
Esophageal Thermal Regulation And Gastric Suctioning Device
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Class 2
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PLA
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§874.5350 |
Device, Antichoke, Suction
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Class 3
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EWT
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§878.4780 |
Pump, Portable, Aspiration (Manual Or Powered)
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Class 2
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BTA
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§878.4780 |
Apparatus, Suction, Ward Use, Portable, Ac-Powered
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Class 2
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JCX
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§878.4780 |
Wound Drain Catheter System
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Class 2
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OTK
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§878.5040 |
System, Suction, Lipoplasty
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Class 2
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MUU
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§878.5040 |
System, Suction, Lipoplasty For Removal
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Class 2
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QPB
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Relevant FDA Guidance and/or Supportive Publications*
1. Guidance for Industry and FDA Reviewers/Staff: Guidance Document for Powered Suction Pump 510(k)s, issued September 1998.
2. ISO 10079-4 First edition 2021-08 Medical suction equipment - Part 4: General requirements.
Appropriate Use of Voluntary Consensus Standards in Premarket Submissions for Medical Devices - Guidance for Industry and Food and Drug Administration Staff, issued September 2018. |
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FDA Technical Contact
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Standards Development Organization
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FDA Specialty Task Group (STG)
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*These are provided as examples and others may be applicable. |