VERSATELL; VERSATELL-S— 510(k) K941959

Name: FDA 510(k) clearance K941959
Creator: U.S. Food and Drug Administration
Published: 1995-06-21

Substantially Equivalent

Progressive Concepts, Inc.

FDA 510(k) clearance K941959 for VERSATELL; VERSATELL-S, Substantially Equivalent on 1995-06-21. Applicant: Progressive Concepts, Inc.. Device class: 2.

Clearance details

Applicant: Progressive Concepts, Inc.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1994-04-22
Decision date: 1995-06-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denton, MD, US

Download summary PDF View on FDA.gov ↗

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