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FDA 510(k)

MINOR LACERATION TRAY W/ INSTRUMENT, STERILE, DISP

K-Number: K920517 · 1992-05-11

ApplicantTrinity Laboratories, Inc.
Decision Date1992-05-11
Product CodeKKX
Advisory CommitteeSU
DecisionUnknown

Device Summary

MINOR LACERATION TRAY W/ INSTRUMENT, STERILE, DISP 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 1992-05-11 under 510(k) number K920517. 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 MINOR LACERATION TRAY W/ INSTRUMENT, STERILE, DISP?

MINOR LACERATION TRAY W/ INSTRUMENT, STERILE, DISP is a medical device that received FDA 510(k) clearance on 1992-05-11. The listed applicant is Trinity Laboratories, Inc.. The 510(k) number is K920517.

When did MINOR LACERATION TRAY W/ INSTRUMENT, STERILE, DISP receive FDA 510(k) clearance?

MINOR LACERATION TRAY W/ INSTRUMENT, STERILE, DISP received FDA 510(k) clearance on 1992-05-11, under 510(k) number K920517.

Who is the listed applicant for MINOR LACERATION TRAY W/ INSTRUMENT, STERILE, DISP?

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 MINOR LACERATION TRAY W/ INSTRUMENT, STERILE, DISP?

The FDA product code for MINOR LACERATION TRAY W/ INSTRUMENT, STERILE, DISP 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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