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FDA 510(k), K182519, Miha Bodytec II
FDA 510(k), K182519, Miha Bodytec II
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$149.00 USD
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510(K) Number: K182519
Device Name: Miha Bodytec II
Manufacturer: Miha Bodytec Gmbh
Device Classification Name: stimulator, muscle, powered, for muscle conditioning
Regulation Number: 890.5850
Classification Product Code: NGX
Date Received: 09/13/2018
Decision Date: 06/07/2019
Regulation Medical Specialty: Physical Medicine
Device Name: Miha Bodytec II
Manufacturer: Miha Bodytec Gmbh
Device Classification Name: stimulator, muscle, powered, for muscle conditioning
Regulation Number: 890.5850
Classification Product Code: NGX
Date Received: 09/13/2018
Decision Date: 06/07/2019
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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