| Part B: Supplementary Information Sheet (SIS) |
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FR Recognition List Number
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029
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Date of Entry 08/20/2012
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FR Recognition Number
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6-242
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| Standard | |
ISO 8536-2 Third edition 2010-03-15 Infusion equipment for medical use - Part 2: Closures for infusion bottles |
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Scope/AbstractISO 8536 2:2010 specifies the shape, dimensions, material, performance requirements and labelling of closures for infusion bottles as specified in ISO 8536-1. The dimensional requirements are not applicable to barrier-coated closures. Closures specified in ISO 8536 2:2010 are intended for single use only. |
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| Extent of Recognition
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Rationale for Recognition
| This standard is relevant to medical devices and is recognized on its scientific and technical merit and/or because it supports existing regulatory policies. |
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Transition Period
| FDA recognition of ISO 8536-2 Third edition 2010-03-15 [Rec# 6-242] will be superseded by recognition of ISO 8536-2 Fourth edition 2023-01 [Rec# 6-506]. FDA will accept declarations of conformity, in support of premarket submissions, to [Rec# 6-242] until July 4, 2027. After this transition period, declarations of conformity to [Rec# 6-242] will not be accepted. |
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Public Law, CFR Citation(s) and Procode(s)*
| Regulation Number |
Device Name |
Device Class |
Product Code |
| §880.5440 |
Set, I.V. Fluid Transfer
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Class 2
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LHI
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Relevant FDA Guidance and/or Supportive Publications*
Guidance for Industry and FDA Staff Intravascular Administration Sets Premarket Notification Submissions [510(k)] Document issued on: July 11, 2008
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)
| General Plastic Surgery/General Hospital |
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| *These are provided as examples and others may be applicable. |