AUTO SUTURE
K-Number: K771589 · 1977-12-13
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Device Summary
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
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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