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FDA 510(k)

LACERATION TRAYS

K-Number: K920341 · 1992-04-23

ApplicantMedikmark, Inc.
Decision Date1992-04-23
Product CodeKKX
Advisory CommitteeSU
DecisionUnknown

Device Summary

LACERATION TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is Medikmark, Inc.. It received FDA 510(k) clearance on 1992-04-23 under 510(k) number K920341. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the LACERATION TRAYS?

LACERATION TRAYS is a medical device that received FDA 510(k) clearance on 1992-04-23. The listed applicant is Medikmark, Inc.. The 510(k) number is K920341.

When did LACERATION TRAYS receive FDA 510(k) clearance?

LACERATION TRAYS received FDA 510(k) clearance on 1992-04-23, under 510(k) number K920341.

Who is the listed applicant for LACERATION TRAYS?

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

What is the FDA product code for LACERATION TRAYS?

The FDA product code for LACERATION TRAYS is KKX.

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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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