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FDA 510(k), K173692, D-Actor 200 Vibration Massage System
FDA 510(k), K173692, D-Actor 200 Vibration Massage System
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510(K) Number: K173692
Device Name: D-Actor 200 Vibration Massage System
Manufacturer: Storz Medical AG
Device Classification Name: massager, therapeutic, electric
Regulation Number: 890.5660
Classification Product Code: ISA
Date Received: 12/01/2017
Decision Date: 04/13/2018
Regulation Medical Specialty: Physical Medicine
Device Name: D-Actor 200 Vibration Massage System
Manufacturer: Storz Medical AG
Device Classification Name: massager, therapeutic, electric
Regulation Number: 890.5660
Classification Product Code: ISA
Date Received: 12/01/2017
Decision Date: 04/13/2018
Regulation Medical Specialty: Physical Medicine
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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