FDA 510(k), K020399, RESPERATE; MODEL RR-150
FDA 510(k), K020399, RESPERATE; MODEL RR-150
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$149.00 USD
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510(K) Number: K020399
Device Name: RESPERATE; MODEL RR-150
Manufacturer:
Device Classification Name: Device, Biofeedback
Regulation Number: 882.5050
Classification Product Code: HCC
Date Received: 02/06/2002
Decision Date: 07/02/2002
Regulation Medical Specialty: Neurology
Device Name: RESPERATE; MODEL RR-150
Manufacturer:
Device Classification Name: Device, Biofeedback
Regulation Number: 882.5050
Classification Product Code: HCC
Date Received: 02/06/2002
Decision Date: 07/02/2002
Regulation Medical Specialty: Neurology