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FDA 510(k)

DELUXE WOUND CLOSURE TRAY, STERILE, DISPOSABLE

K-Number: K921204 · 1992-08-13

ApplicantTrinity Laboratories, Inc.
Decision Date1992-08-13
Product CodeKKX
Advisory CommitteeSU
DecisionUnknown

Device Summary

DELUXE WOUND CLOSURE TRAY, STERILE, DISPOSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Trinity Laboratories, Inc.. It received FDA 510(k) clearance on 1992-08-13 under 510(k) number K921204. 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 DELUXE WOUND CLOSURE TRAY, STERILE, DISPOSABLE?

DELUXE WOUND CLOSURE TRAY, STERILE, DISPOSABLE is a medical device that received FDA 510(k) clearance on 1992-08-13. The listed applicant is Trinity Laboratories, Inc.. The 510(k) number is K921204.

When did DELUXE WOUND CLOSURE TRAY, STERILE, DISPOSABLE receive FDA 510(k) clearance?

DELUXE WOUND CLOSURE TRAY, STERILE, DISPOSABLE received FDA 510(k) clearance on 1992-08-13, under 510(k) number K921204.

Who is the listed applicant for DELUXE WOUND CLOSURE TRAY, STERILE, DISPOSABLE?

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

What is the FDA product code for DELUXE WOUND CLOSURE TRAY, STERILE, DISPOSABLE?

The FDA product code for DELUXE WOUND CLOSURE TRAY, STERILE, DISPOSABLE is KKX.

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Other records listing Trinity Laboratories, Inc. as applicant

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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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