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FDA 510(k), K202079, Physiq
FDA 510(k), K202079, Physiq
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510(K) Number: K202079
Device Name: Physiq
Manufacturer: El. En. Electronic Engineering SPA
Device Classification Name: Stimulator, Muscle, Powered
Regulation Number: 890.5850
Classification Product Code: IPF
Date Received: 07/27/2020
Decision Date: 11/25/2020
Regulation Medical Specialty: Physical Medicine
Device Name: Physiq
Manufacturer: El. En. Electronic Engineering SPA
Device Classification Name: Stimulator, Muscle, Powered
Regulation Number: 890.5850
Classification Product Code: IPF
Date Received: 07/27/2020
Decision Date: 11/25/2020
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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