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FDA 510(k)

AUTO SUTURE

K-Number: K771589 · 1977-12-13

Decision Date1977-12-13
Product CodeGDJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AUTO SUTURE is the device name listed in this FDA 510(k) record. The listed applicant is U. S. Surgical Corp.. It received FDA 510(k) clearance on 1977-12-13 under 510(k) number K771589. The device is classified under product code GDJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO SUTURE?

AUTO SUTURE is a medical device that received FDA 510(k) clearance on 1977-12-13. The listed applicant is U. S. Surgical Corp.. The 510(k) number is K771589.

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

AUTO SUTURE received FDA 510(k) clearance on 1977-12-13, under 510(k) number K771589.

Who is the listed applicant for AUTO SUTURE?

The FDA 510(k) record lists U. S. Surgical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTO SUTURE?

The FDA product code for AUTO SUTURE is GDJ.

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 U. S. Surgical Corp. 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.

Related Devices (Code: GDJ)

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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