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FDA 510(k)

POST SURGICAL KIT/POST BIOPSY KIT

K-Number: K910011 · 1991-03-27

ApplicantDermatological Research Laboratories, Inc.
Decision Date1991-03-27
Product CodeMCY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POST SURGICAL KIT/POST BIOPSY KIT is the device name listed in this FDA 510(k) record. The listed applicant is Dermatological Research Laboratories, Inc.. It received FDA 510(k) clearance on 1991-03-27 under 510(k) number K910011. The device is classified under product code MCY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POST SURGICAL KIT/POST BIOPSY KIT?

POST SURGICAL KIT/POST BIOPSY KIT is a medical device that received FDA 510(k) clearance on 1991-03-27. The listed applicant is Dermatological Research Laboratories, Inc.. The 510(k) number is K910011.

When did POST SURGICAL KIT/POST BIOPSY KIT receive FDA 510(k) clearance?

POST SURGICAL KIT/POST BIOPSY KIT received FDA 510(k) clearance on 1991-03-27, under 510(k) number K910011.

Who is the listed applicant for POST SURGICAL KIT/POST BIOPSY KIT?

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

What is the FDA product code for POST SURGICAL KIT/POST BIOPSY KIT?

The FDA product code for POST SURGICAL KIT/POST BIOPSY KIT is MCY.

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Related Devices (Code: MCY)

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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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