RICHARD-ALLAN VESSEL LOOPS— 510(k) K900566

Name: FDA 510(k) clearance K900566
Creator: U.S. Food and Drug Administration
Published: 1990-05-03

Substantially Equivalent

Richard-Allan Medical Ind., Inc.

FDA 510(k) clearance K900566 for RICHARD-ALLAN VESSEL LOOPS, Substantially Equivalent on 1990-05-03. Applicant: Richard-Allan Medical Ind., Inc.. Device class: 1.

Clearance details

Applicant: Richard-Allan Medical Ind., Inc.
Product code: Code KDC
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1990-02-07
Decision date: 1990-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Richland, MI, US

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