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FDA 510(k)

METRONIDAZOLE DISCS

K-Number: K801805 · 1981-02-10

ApplicantG.D. Searle and Co.
Decision Date1981-02-10
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

METRONIDAZOLE DISCS is the device name listed in this FDA 510(k) record. The listed applicant is G.D. Searle and Co.. It received FDA 510(k) clearance on 1981-02-10 under 510(k) number K801805. The device is classified under product code JWY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the METRONIDAZOLE DISCS?

METRONIDAZOLE DISCS is a medical device that received FDA 510(k) clearance on 1981-02-10. The listed applicant is G.D. Searle and Co.. The 510(k) number is K801805.

When did METRONIDAZOLE DISCS receive FDA 510(k) clearance?

METRONIDAZOLE DISCS received FDA 510(k) clearance on 1981-02-10, under 510(k) number K801805.

Who is the listed applicant for METRONIDAZOLE DISCS?

The FDA 510(k) record lists G.D. Searle and Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for METRONIDAZOLE DISCS?

The FDA product code for METRONIDAZOLE DISCS is JWY.

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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.

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