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FDA 510(k)

LACERATION TRAY

K-Number: K960520 · 1996-03-21

ApplicantMedco Instruments, Inc.
Decision Date1996-03-21
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LACERATION TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Medco Instruments, Inc.. It received FDA 510(k) clearance on 1996-03-21 under 510(k) number K960520. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LACERATION TRAY?

LACERATION TRAY is a medical device that received FDA 510(k) clearance on 1996-03-21. The listed applicant is Medco Instruments, Inc.. The 510(k) number is K960520.

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

LACERATION TRAY received FDA 510(k) clearance on 1996-03-21, under 510(k) number K960520.

Who is the listed applicant for LACERATION TRAY?

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

What is the FDA product code for LACERATION TRAY?

The FDA product code for LACERATION TRAY is FRG.

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Related Devices (Code: FRG)

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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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