CATHETER, INTRAVASCULAR (ARGYLE IV SK)— 510(k) K760760

Name: FDA 510(k) clearance K760760
Creator: U.S. Food and Drug Administration
Published: 1976-12-09

Substantially Equivalent

Sherwood Medical Industries

FDA 510(k) clearance K760760 for CATHETER, INTRAVASCULAR (ARGYLE IV SK), Substantially Equivalent on 1976-12-09. Applicant: Sherwood Medical Industries. Device class: 1.

Clearance details

Applicant: Sherwood Medical Industries
Product code: Code JCY
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1976-10-04
Decision date: 1976-12-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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