AUTO SUTURE GAS POWERED DISP. LDS STAPL— 510(k) K810188

Name: FDA 510(k) clearance K810188
Creator: U.S. Food and Drug Administration
Published: 1981-03-20

Substantially Equivalent

United States Surgical, A Division of Tyco Healthc

FDA 510(k) clearance K810188 for AUTO SUTURE GAS POWERED DISP. LDS STAPL, Substantially Equivalent on 1981-03-20. 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 KBC
Device class: Class 1
Regulation: 21 CFR 874.4420
Advisory panel: Ear, Nose, Throat
Date received: 1981-01-22
Decision date: 1981-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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