AUTO SUTURE SURGIPORT SPIRAL SLEEVE— 510(k) K900123

Name: FDA 510(k) clearance K900123
Creator: U.S. Food and Drug Administration
Published: 1990-04-04

Substantially Equivalent

United States Surgical, A Division of Tyco Healthc

FDA 510(k) clearance K900123 for AUTO SUTURE SURGIPORT SPIRAL SLEEVE, Substantially Equivalent on 1990-04-04. Applicant: United States Surgical, A Division of Tyco Healthc. Device class: 2.

Clearance details

Applicant: United States Surgical, A Division of Tyco Healthc
Product code: Code FBQ
Device class: Class 2
Regulation: 21 CFR 876.5090
Advisory panel: Gastroenterology, Urology
Date received: 1990-01-09
Decision date: 1990-04-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwalk, CT, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.