ARTHROPHONOMETER— 510(k) K862286

Substantially Equivalent

Arthrotek, Inc.

FDA 510(k) clearance K862286 for ARTHROPHONOMETER, Substantially Equivalent on 1987-01-07. Applicant: Arthrotek, Inc..

Clearance details

Applicant: Arthrotek, Inc.
Product code: Code NFQ
Advisory panel: Dental
Date received: 1986-06-16
Decision date: 1987-01-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Hartford, CT, US

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