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FDA 510(k)

FORCEPS, SUTURE, AUTO

K-Number: K772286 · 1977-12-20

ApplicantHartmann Group, Inc.
Decision Date1977-12-20
Product CodeGDO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FORCEPS, SUTURE, AUTO is the device name listed in this FDA 510(k) record. The listed applicant is Hartmann Group, Inc.. It received FDA 510(k) clearance on 1977-12-20 under 510(k) number K772286. The device is classified under product code GDO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORCEPS, SUTURE, AUTO?

FORCEPS, SUTURE, AUTO is a medical device that received FDA 510(k) clearance on 1977-12-20. The listed applicant is Hartmann Group, Inc.. The 510(k) number is K772286.

When did FORCEPS, SUTURE, AUTO receive FDA 510(k) clearance?

FORCEPS, SUTURE, AUTO received FDA 510(k) clearance on 1977-12-20, under 510(k) number K772286.

Who is the listed applicant for FORCEPS, SUTURE, AUTO?

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

What is the FDA product code for FORCEPS, SUTURE, AUTO?

The FDA product code for FORCEPS, SUTURE, AUTO is GDO.

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Related Devices (Code: GDO)

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.

K926199UNICLIP SURGICAL CLIP APPLIERUnisurge, Inc.K890941MODIFIED SUTURE DISP. ENDOSCOPIC SURGICAL CLIP APPUnited States Surgical, A Division of Tyco HealthcK890159TOWEL CLIPSDhason Brothers, Inc.K890233SUTURE CLIP APPLIER/REMOVERKinetic Medical ProductsK820837DISPOSABLE MULTIPLE LIGATING CLIPETHICON, Inc.K812291ETHICON MULTIPLE LIGATING CLIP APPLIERETHICON, 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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