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FDA 510(k)

BAYONET SURGICAL INSTRUMENTS

K-Number: K772371 · 1978-01-06

ApplicantEdward Weck, Inc.
Decision Date1978-01-06
Product CodeHAO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

BAYONET SURGICAL INSTRUMENTS 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 1978-01-06 under 510(k) number K772371. The device is classified under product code HAO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BAYONET SURGICAL INSTRUMENTS?

BAYONET SURGICAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1978-01-06. The listed applicant is Edward Weck, Inc.. The 510(k) number is K772371.

When did BAYONET SURGICAL INSTRUMENTS receive FDA 510(k) clearance?

BAYONET SURGICAL INSTRUMENTS received FDA 510(k) clearance on 1978-01-06, under 510(k) number K772371.

Who is the listed applicant for BAYONET SURGICAL INSTRUMENTS?

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 BAYONET SURGICAL INSTRUMENTS?

The FDA product code for BAYONET SURGICAL INSTRUMENTS is HAO.

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Other records listing Edward Weck, Inc. as applicant

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

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Related Devices (Code: HAO)

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.

K220920Matreneu Percutaneous Balloon Compression KitShenzhen Shineyard Medical Device Co. , Ltd.K940973MULLAN GANGLION MICROCOMPRESSION SETCook, Inc.K951492RIB RESECTORUnited States Surgical, A Division of Tyco HealthcK943115AUTO SUTURE PITUITARY SPINAL RONGEURUnited States Surgical, A Division of Tyco HealthcK942968AUTO SUTURE SPINAL OSTEOTOMEUnited States Surgical, A Division of Tyco HealthcK942967AUTO SUTURE SPINAL CURETTEUnited States Surgical, A Division of Tyco Healthc

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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