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FDA 510(k)

WECK RACK (STERILIZING ACCESSORY TRAY)

K-Number: K791743 · 1979-09-26

ApplicantEdward Weck, Inc.
Decision Date1979-09-26
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WECK RACK (STERILIZING ACCESSORY TRAY) is the device name listed in this FDA 510(k) record. The listed applicant is Edward Weck, Inc.. It received FDA 510(k) clearance on 1979-09-26 under 510(k) number K791743. 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 WECK RACK (STERILIZING ACCESSORY TRAY)?

WECK RACK (STERILIZING ACCESSORY TRAY) is a medical device that received FDA 510(k) clearance on 1979-09-26. The listed applicant is Edward Weck, Inc.. The 510(k) number is K791743.

When did WECK RACK (STERILIZING ACCESSORY TRAY) receive FDA 510(k) clearance?

WECK RACK (STERILIZING ACCESSORY TRAY) received FDA 510(k) clearance on 1979-09-26, under 510(k) number K791743.

Who is the listed applicant for WECK RACK (STERILIZING ACCESSORY TRAY)?

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

What is the FDA product code for WECK RACK (STERILIZING ACCESSORY TRAY)?

The FDA product code for WECK RACK (STERILIZING ACCESSORY TRAY) is FSM.

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Other records listing Edward Weck, Inc. as applicant

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.

K915378WECK TROCARK914690LM15(TM), CATALOG NUMBER - 523821K911915HEMOCLIP IIK914470PNEUMO-SEAL(TM)K911272ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705K902108HEM-O-LOK(TM)

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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.

K971217INSTRUMENT TRAY LINERGeneral Hospital Supply Corp.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.

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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