BOWEN PROBE— 510(k) K863149

Substantially Equivalent

Bowen & Company, Inc.

FDA 510(k) clearance K863149 for BOWEN PROBE, Substantially Equivalent on 1986-09-05. Applicant: Bowen & Company, Inc..

Clearance details

Applicant: Bowen & Company, Inc.
Product code: Code HXB
Advisory panel: Orthopedic
Date received: 1986-08-15
Decision date: 1986-09-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rockville, MD, US

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