CSD 200/300/400/500 DYNAMOMETER— 510(k) K931321

Name: FDA 510(k) clearance K931321
Creator: U.S. Food and Drug Administration
Published: 1994-02-15

Substantially Equivalent

John Chatillon & Sons, Inc.

FDA 510(k) clearance K931321 for CSD 200/300/400/500 DYNAMOMETER, Substantially Equivalent on 1994-02-15. Applicant: John Chatillon & Sons, Inc.. Device class: 2.

Clearance details

Applicant: John Chatillon & Sons, Inc.
Product code: Code LBB
Device class: Class 2
Regulation: 21 CFR 888.1240
Advisory panel: Orthopedic
Date received: 1993-03-16
Decision date: 1994-02-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Greensboro, NC, US

Download summary PDF View on FDA.gov ↗

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