DYNAMOMETER— 510(k) K964685

Substantially Equivalent

John Chatillon & Sons, Inc.

FDA 510(k) clearance K964685 for DYNAMOMETER, Substantially Equivalent on 1997-01-27. 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: 1996-11-22
Decision date: 1997-01-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Greensboro, NC, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.