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FDA 510(k)

CODE 17-ENDOSCOPE DEODORANT

K-Number: K840208 · 1984-07-19

ApplicantKnox Laboratories
Decision Date1984-07-19
Product CodeFEB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CODE 17-ENDOSCOPE DEODORANT is the device name listed in this FDA 510(k) record. The listed applicant is Knox Laboratories. It received FDA 510(k) clearance on 1984-07-19 under 510(k) number K840208. The device is classified under product code FEB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODE 17-ENDOSCOPE DEODORANT?

CODE 17-ENDOSCOPE DEODORANT is a medical device that received FDA 510(k) clearance on 1984-07-19. The listed applicant is Knox Laboratories. The 510(k) number is K840208.

When did CODE 17-ENDOSCOPE DEODORANT receive FDA 510(k) clearance?

CODE 17-ENDOSCOPE DEODORANT received FDA 510(k) clearance on 1984-07-19, under 510(k) number K840208.

Who is the listed applicant for CODE 17-ENDOSCOPE DEODORANT?

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

What is the FDA product code for CODE 17-ENDOSCOPE DEODORANT?

The FDA product code for CODE 17-ENDOSCOPE DEODORANT is FEB.

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Official Source

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

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