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FDA 510(k), K021100, 300 PV COMPLETE ELECTROTHERAPY SYSTEM
FDA 510(k), K021100, 300 PV COMPLETE ELECTROTHERAPY SYSTEM
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$49.00 USD
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510(K) Number: K021100
Device Name: 300 PV COMPLETE ELECTROTHERAPY SYSTEM
Manufacturer: EMPI
Device Classification Name: stimulator, muscle, powered
Regulation Number: 890.5850
Classification Product Code: IPF
Date Received: 04/04/2002
Decision Date: 06/18/2002
Regulation Medical Specialty: Physical Medicine
Device Name: 300 PV COMPLETE ELECTROTHERAPY SYSTEM
Manufacturer: EMPI
Device Classification Name: stimulator, muscle, powered
Regulation Number: 890.5850
Classification Product Code: IPF
Date Received: 04/04/2002
Decision Date: 06/18/2002
Regulation Medical Specialty: Physical Medicine
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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