1
/
of
0
FDA 510(k), K062532, ELECTROPULSE - LOW BACK PAIN
FDA 510(k), K062532, ELECTROPULSE - LOW BACK PAIN
Regular price
$149.00 USD
Regular price
Sale price
$149.00 USD
Unit price
/
per
510(K) Number: K062532
Device Name: ELECTROPULSE - LOW BACK PAIN
Manufacturer: PAIN RELIEF TECHNOLOGIES
Device Classification Name: stimulator, nerve, transcutaneous, over-the-counter
Regulation Number: 882.5890
Classification Product Code: NUH
Date Received: 08/28/2006
Decision Date: 02/09/2007
Regulation Medical Specialty: Neurology
Device Name: ELECTROPULSE - LOW BACK PAIN
Manufacturer: PAIN RELIEF TECHNOLOGIES
Device Classification Name: stimulator, nerve, transcutaneous, over-the-counter
Regulation Number: 882.5890
Classification Product Code: NUH
Date Received: 08/28/2006
Decision Date: 02/09/2007
Regulation Medical Specialty: Neurology
Couldn't load pickup availability
- 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.
View full details