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FDA 510(k)

SUTURE TISSUE APPROXIMATING FORCEP

K-Number: K771515 · 1977-09-30

Decision Date1977-09-30
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUTURE TISSUE APPROXIMATING FORCEP is the device name listed in this FDA 510(k) record. The listed applicant is United States Surgical, A Division of Tyco Healthc. It received FDA 510(k) clearance on 1977-09-30 under 510(k) number K771515. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUTURE TISSUE APPROXIMATING FORCEP?

SUTURE TISSUE APPROXIMATING FORCEP is a medical device that received FDA 510(k) clearance on 1977-09-30. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K771515.

When did SUTURE TISSUE APPROXIMATING FORCEP receive FDA 510(k) clearance?

SUTURE TISSUE APPROXIMATING FORCEP received FDA 510(k) clearance on 1977-09-30, under 510(k) number K771515.

Who is the listed applicant for SUTURE TISSUE APPROXIMATING FORCEP?

The FDA 510(k) record lists United States Surgical, A Division of Tyco Healthc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUTURE TISSUE APPROXIMATING FORCEP?

The FDA product code for SUTURE TISSUE APPROXIMATING FORCEP is GEN.

Related Clinical Trials

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.

Other records listing United States Surgical, A Division of Tyco Healthc 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.

View all 218 devices →

Related Devices (Code: GEN)

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.

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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