MEDIFETTE ERGOMETER— 510(k) K850870

Substantially Equivalent

Ketronic, Inc.

FDA 510(k) clearance K850870 for MEDIFETTE ERGOMETER, Substantially Equivalent on 1985-06-12. Applicant: Ketronic, Inc..

Clearance details

Applicant: Ketronic, Inc.
Advisory panel: Unknown
Date received: 1985-03-01
Decision date: 1985-06-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: The Netherlands, NL

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