ARTROMOT MULTI DIRECTIONAL ANKLE CPM— 510(k) K924484

Substantially Equivalent

Buckman Co., Inc.

FDA 510(k) clearance K924484 for ARTROMOT MULTI DIRECTIONAL ANKLE CPM, Substantially Equivalent on 1993-03-22. Applicant: Buckman Co., Inc..

Clearance details

Applicant: Buckman Co., Inc.
Product code: Code BXB
Advisory panel: Physical Medicine
Date received: 1992-09-03
Decision date: 1993-03-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Concord, CA, US

Download summary PDF View on FDA.gov ↗

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