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FDA 510(k)

INSTRUMENT TRAY LINER

K-Number: K971217 · 1997-05-06

ApplicantGeneral Hospital Supply Corp.
Decision Date1997-05-06
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INSTRUMENT TRAY LINER is the device name listed in this FDA 510(k) record. The listed applicant is General Hospital Supply Corp.. It received FDA 510(k) clearance on 1997-05-06 under 510(k) number K971217. The device is classified under product code FSM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTRUMENT TRAY LINER?

INSTRUMENT TRAY LINER is a medical device that received FDA 510(k) clearance on 1997-05-06. The listed applicant is General Hospital Supply Corp.. The 510(k) number is K971217.

When did INSTRUMENT TRAY LINER receive FDA 510(k) clearance?

INSTRUMENT TRAY LINER received FDA 510(k) clearance on 1997-05-06, under 510(k) number K971217.

Who is the listed applicant for INSTRUMENT TRAY LINER?

The FDA 510(k) record lists General Hospital Supply Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSTRUMENT TRAY LINER?

The FDA product code for INSTRUMENT TRAY LINER is FSM.

Related Clinical Trials

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Related Devices (Code: FSM)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K962328SINGLE USE INSTRUMENT TRAYMedcare Medical Group, Inc.K944025SURGICAL INSTRUMENT TRAYRiley Medical, Inc.K912106ARTHROSCOPY TRAYMedical Device Inspection Co., Inc.K912053OPEN HEART TRAYMedical Device Inspection Co., Inc.K912052HEART CATH TRAYMedical Device Inspection Co., Inc.K912104MAJOR BASIN TRAYMedical Device Inspection Co., Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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