CONPHAR DUAL HEAD STETHOSCOPE— 510(k) K801183

Substantially Equivalent

Conphar, Inc.

FDA 510(k) clearance K801183 for CONPHAR DUAL HEAD STETHOSCOPE, Substantially Equivalent on 1980-06-04. Applicant: Conphar, Inc..

Clearance details

Applicant: Conphar, Inc.
Product code: Code LDE
Advisory panel: Cardiovascular
Date received: 1980-05-16
Decision date: 1980-06-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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