DANNIFLEX CPM 880(TM)— 510(k) K900581

Substantially Equivalent

Buckman Co., Inc.

FDA 510(k) clearance K900581 for DANNIFLEX CPM 880(TM), Substantially Equivalent on 1990-02-20. Applicant: Buckman Co., Inc..

Clearance details

Applicant: Buckman Co., Inc.
Product code: Code JFA
Advisory panel: Physical Medicine
Date received: 1990-02-07
Decision date: 1990-02-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Concord, CA, US

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