AUTO SUTURE POLY GIA SURGICAL STAPLER
K-Number: K843603 · 1984-10-31
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Device Summary
Frequently Asked Questions
What is the AUTO SUTURE POLY GIA SURGICAL STAPLER?
AUTO SUTURE POLY GIA SURGICAL STAPLER is a medical device that received FDA 510(k) clearance on 1984-10-31. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K843603.
When did AUTO SUTURE POLY GIA SURGICAL STAPLER receive FDA 510(k) clearance?
AUTO SUTURE POLY GIA SURGICAL STAPLER received FDA 510(k) clearance on 1984-10-31, under 510(k) number K843603.
Who is the listed applicant for AUTO SUTURE POLY GIA SURGICAL STAPLER?
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 AUTO SUTURE POLY GIA SURGICAL STAPLER?
The FDA product code for AUTO SUTURE POLY GIA SURGICAL STAPLER is GDW.
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.
Related Devices (Code: GDW)
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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