Part B: Supplementary Information Sheet (SIS) |
FR Recognition List Number
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019
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Date of Entry 12/19/2007
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FR Recognition Number
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10-37
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Standard | |
ISO 10942 Second edition 2006-06-01 Ophthalmic instruments - Direct ophthalmoscopes |
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Scope/AbstractThis International Standard, together with ISO 15004-1 and ISO 15004-2, specifies minimum requirements and test methods for hand-held direct ophthalmoscopes designed for directly observing the eye fundus.
This International Standard takes precedence over ISO 15004-1 and ISO 15004-2, if differences exist. |
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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FDA recognition of ISO 10942 Second edition 2006-06-01 [Rec# 10-37] will be superseded by recognition of ISO 10942 Third edition 2022-01 [Rec# 10-132]. FDA will accept declarations of conformity, in support of premarket submissions, to [Rec# 10-37] until December 17, 2023. After this transition period, declarations of conformity to [Rec# 10-37] will not be accepted. |
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Public Law, CFR Citation(s) and Procode(s)*
Regulation Number |
Device Name |
Device Class |
Product Code |
§886.1570 |
Ophthalmoscope, Battery-Powered |
Class 2 |
HLJ |
§886.1570 |
Ophthalmoscope, Laser, Scanning |
Class 2 |
MYC |
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Relevant FDA Guidance and/or Supportive Publications*
Guidance for Industry Ophthalmoscope Guidance - (Direct and Indirect), issued July 1998.
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. |