AUTO SUTURE DISP. ENDOSCOPIC SURG. CLIP APPLIER
K-Number: K883018 · 1988-08-03
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Device Summary
Frequently Asked Questions
What is the AUTO SUTURE DISP. ENDOSCOPIC SURG. CLIP APPLIER?
AUTO SUTURE DISP. ENDOSCOPIC SURG. CLIP APPLIER is a medical device that received FDA 510(k) clearance on 1988-08-03. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K883018.
When did AUTO SUTURE DISP. ENDOSCOPIC SURG. CLIP APPLIER receive FDA 510(k) clearance?
AUTO SUTURE DISP. ENDOSCOPIC SURG. CLIP APPLIER received FDA 510(k) clearance on 1988-08-03, under 510(k) number K883018.
Who is the listed applicant for AUTO SUTURE DISP. ENDOSCOPIC SURG. CLIP APPLIER?
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 DISP. ENDOSCOPIC SURG. CLIP APPLIER?
The FDA product code for AUTO SUTURE DISP. ENDOSCOPIC SURG. CLIP APPLIER is FZP.
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: FZP)
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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