FDA 510(k)

AO FLEXIBLE FIBER OPTIC S/COLONOSCOPE

K-Number: K792179 · 1979-12-06

Decision Date1979-12-06

Product CodeFDF

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

AO FLEXIBLE FIBER OPTIC S/COLONOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is American Optical Corp.. It received FDA 510(k) clearance on 1979-12-06 under 510(k) number K792179. The device is classified under product code FDF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AO FLEXIBLE FIBER OPTIC S/COLONOSCOPE?

AO FLEXIBLE FIBER OPTIC S/COLONOSCOPE is a medical device that received FDA 510(k) clearance on 1979-12-06. The listed applicant is American Optical Corp.. The 510(k) number is K792179.

When did AO FLEXIBLE FIBER OPTIC S/COLONOSCOPE receive FDA 510(k) clearance?

AO FLEXIBLE FIBER OPTIC S/COLONOSCOPE received FDA 510(k) clearance on 1979-12-06, under 510(k) number K792179.

Who is the listed applicant for AO FLEXIBLE FIBER OPTIC S/COLONOSCOPE?

The FDA 510(k) record lists American Optical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AO FLEXIBLE FIBER OPTIC S/COLONOSCOPE?

The FDA product code for AO FLEXIBLE FIBER OPTIC S/COLONOSCOPE is FDF.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.