DANNIFLEX 400I— 510(k) K870510

Substantially Equivalent

Buckman Co., Inc.

FDA 510(k) clearance K870510 for DANNIFLEX 400I, Substantially Equivalent on 1987-02-26. Applicant: Buckman Co., Inc..

Clearance details

Applicant: Buckman Co., Inc.
Product code: Code BXB
Advisory panel: Physical Medicine
Date received: 1987-02-05
Decision date: 1987-02-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Martinez, CA, US

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