MODIFIED AUTO SUTURE PURSTRING DISP. AUTOMATIC— 510(k) K901107

Name: FDA 510(k) clearance K901107
Creator: U.S. Food and Drug Administration
Published: 1990-04-09

Substantially Equivalent

United States Surgical, A Division of Tyco Healthc

FDA 510(k) clearance K901107 for MODIFIED AUTO SUTURE PURSTRING DISP. AUTOMATIC, Substantially Equivalent on 1990-04-09. Applicant: United States Surgical, A Division of Tyco Healthc. Device class: 1.

Clearance details

Applicant: United States Surgical, A Division of Tyco Healthc
Product code: Code GDJ
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1990-03-08
Decision date: 1990-04-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwalk, CT, US

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