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FDA 510(k)

INCISSION & DRAINAGE TRAY

K-Number: K921203 · 1992-08-13

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

Device Summary

INCISSION & DRAINAGE TRAY 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 K921203. 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 INCISSION & DRAINAGE TRAY?

INCISSION & DRAINAGE TRAY 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 K921203.

When did INCISSION & DRAINAGE TRAY receive FDA 510(k) clearance?

INCISSION & DRAINAGE TRAY received FDA 510(k) clearance on 1992-08-13, under 510(k) number K921203.

Who is the listed applicant for INCISSION & DRAINAGE TRAY?

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 INCISSION & DRAINAGE TRAY?

The FDA product code for INCISSION & DRAINAGE TRAY is KKX.

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Other records listing Trinity Laboratories, Inc. as applicant

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Related Devices (Code: 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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