FDA 510(k), K952164, EMI MODEL FFF-IA
FDA 510(k), K952164, EMI MODEL FFF-IA
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510(K) Number: K952164
Device Name: EMI MODEL FFF-IA
Manufacturer:
Device Classification Name: Computer, Diagnostic, Programmable
Regulation Number: 870.1425
Classification Product Code: DQK
Date Received: 05/03/1995
Decision Date: 05/10/1995
Regulation Medical Specialty: Cardiovascular
Device Name: EMI MODEL FFF-IA
Manufacturer:
Device Classification Name: Computer, Diagnostic, Programmable
Regulation Number: 870.1425
Classification Product Code: DQK
Date Received: 05/03/1995
Decision Date: 05/10/1995
Regulation Medical Specialty: Cardiovascular