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FDA 510(k)

LOWMAN BONE FORCEP

K-Number: K771192 · 1977-07-11

ApplicantEdward Weck, Inc.
Decision Date1977-07-11
Product CodeHTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LOWMAN BONE FORCEP 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 1977-07-11 under 510(k) number K771192. The device is classified under product code HTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOWMAN BONE FORCEP?

LOWMAN BONE FORCEP is a medical device that received FDA 510(k) clearance on 1977-07-11. The listed applicant is Edward Weck, Inc.. The 510(k) number is K771192.

When did LOWMAN BONE FORCEP receive FDA 510(k) clearance?

LOWMAN BONE FORCEP received FDA 510(k) clearance on 1977-07-11, under 510(k) number K771192.

Who is the listed applicant for LOWMAN BONE FORCEP?

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 LOWMAN BONE FORCEP?

The FDA product code for LOWMAN BONE FORCEP is HTD.

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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: HTD)

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.

K051281THE NEEDLE CATCHERE.D.Medical , Ltd.K974595CUSHING BAYONET, INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K974594SEMKIN BIPOLAR FORCEPTitan Mfg., Inc.K974593SEMKIN INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K913964MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPSMarlo Surgical TechnologyK911180CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPSNorthgate Technologies, 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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