DANNIFLEX MODEL 500TM CPM— 510(k) K904735

Substantially Equivalent

Buckman Co., Inc.

FDA 510(k) clearance K904735 for DANNIFLEX MODEL 500TM CPM, Substantially Equivalent on 1991-01-30. Applicant: Buckman Co., Inc..

Clearance details

Applicant: Buckman Co., Inc.
Product code: Code BXB
Advisory panel: Physical Medicine
Date received: 1990-10-17
Decision date: 1991-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Concord, CA, US

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