MODIFIED AUTO SUTURE ENDOSCOPIC GIA SURG. STAPLER*
K-Number: K900129 · 1990-02-27
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Device Summary
Frequently Asked Questions
What is the MODIFIED AUTO SUTURE ENDOSCOPIC GIA SURG. STAPLER*?
MODIFIED AUTO SUTURE ENDOSCOPIC GIA SURG. STAPLER* is a medical device that received FDA 510(k) clearance on 1990-02-27. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K900129.
When did MODIFIED AUTO SUTURE ENDOSCOPIC GIA SURG. STAPLER* receive FDA 510(k) clearance?
MODIFIED AUTO SUTURE ENDOSCOPIC GIA SURG. STAPLER* received FDA 510(k) clearance on 1990-02-27, under 510(k) number K900129.
Who is the listed applicant for MODIFIED AUTO SUTURE ENDOSCOPIC GIA SURG. 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 MODIFIED AUTO SUTURE ENDOSCOPIC GIA SURG. STAPLER*?
The FDA product code for MODIFIED AUTO SUTURE ENDOSCOPIC GIA SURG. 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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