STETHOSCOPE— 510(k) K904547

Substantially Equivalent

Kimball Industries Co., Ltd.

FDA 510(k) clearance K904547 for STETHOSCOPE, Substantially Equivalent on 1991-03-21. Applicant: Kimball Industries Co., Ltd..

Clearance details

Applicant: Kimball Industries Co., Ltd.
Product code: Code LDE
Advisory panel: Cardiovascular
Date received: 1990-10-03
Decision date: 1991-03-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shirley, NY, US

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