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FDA 510(k)

MICRO CLIP STERILIZING CASE #65199

K-Number: K801470 · 1980-07-14

ApplicantEdward Weck, Inc.
Decision Date1980-07-14
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICRO CLIP STERILIZING CASE #65199 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 1980-07-14 under 510(k) number K801470. 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 MICRO CLIP STERILIZING CASE #65199?

MICRO CLIP STERILIZING CASE #65199 is a medical device that received FDA 510(k) clearance on 1980-07-14. The listed applicant is Edward Weck, Inc.. The 510(k) number is K801470.

When did MICRO CLIP STERILIZING CASE #65199 receive FDA 510(k) clearance?

MICRO CLIP STERILIZING CASE #65199 received FDA 510(k) clearance on 1980-07-14, under 510(k) number K801470.

Who is the listed applicant for MICRO CLIP STERILIZING CASE #65199?

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 MICRO CLIP STERILIZING CASE #65199?

The FDA product code for MICRO CLIP STERILIZING CASE #65199 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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