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FDA 510(k)

AUTO SUTURE DISPOS., EEA SURG. STAPLER

K-Number: K802611 · 1980-11-12

ApplicantU. S. Surgical Corp.
Decision Date1980-11-12
Product CodeGAG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AUTO SUTURE DISPOS., EEA SURG. STAPLER 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 1980-11-12 under 510(k) number K802611. The device is classified under product code GAG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO SUTURE DISPOS., EEA SURG. STAPLER?

AUTO SUTURE DISPOS., EEA SURG. STAPLER is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is U. S. Surgical Corp.. The 510(k) number is K802611.

When did AUTO SUTURE DISPOS., EEA SURG. STAPLER receive FDA 510(k) clearance?

AUTO SUTURE DISPOS., EEA SURG. STAPLER received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802611.

Who is the listed applicant for AUTO SUTURE DISPOS., EEA SURG. STAPLER?

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 DISPOS., EEA SURG. STAPLER?

The FDA product code for AUTO SUTURE DISPOS., EEA SURG. STAPLER is GAG.

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.

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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.

K771589AUTO SUTURE

Related Devices (Code: GAG)

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.

K253527Tri-Staple™ 2.0 Black Circular Reload 21mm Extra Thick (SIGCIR21XT); Tri-Staple™ 2.0 Black Circular Reload 25mm Extra Thick (SIGCIR25XT)Covidien, LLCK251482AEON™ Endoscopic Powered StaplerLexington Medical, Inc.K243596da Vinci SP SureForm 45 Staplers and Reloads (SP1098)Intuitive Surgical, Inc.K240881Signia™ Circular Adapter (Standard Length) (SIGCIRSTND); Signia™ Circular Adapter XL Length (SIGCIRXL)Covidien (Part of Medtronic)K241629ECHELON 3000 45mm Compact Stapler (ECH45C); Echelon 3000 45mm Standard Stapler (ECH45S); Echelon 3000 45mm Long Stapler (ECH45L); Echelon 3000 60mm Compact Stapler (ECH60C); Echelon 3000 60mm Standard Stapler (ECH60S); Echelon 3000 60mm Long Stapler (ECH60L)Ethicon Endo-Surgery, LLCK234039AEON Endoscopic Powered Stapler (Short/AEPH060); AEON Endoscopic Powered Stapler (Medium/AEPH160); AEON Endoscopic Powered Stapler (Long/AEPH260)Lexington Medical, 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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