ELECTROPULSE - LOW BACK PAIN— 510(k) K062532
Substantially EquivalentPain Relief Technologies
FDA 510(k) clearance K062532 for ELECTROPULSE - LOW BACK PAIN, Substantially Equivalent on 2007-02-09. Applicant: Pain Relief Technologies. Device class: 2.
Clearance details
- Applicant
- Pain Relief Technologies
- Product code
- Code NUH
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Beaverton, OR, US
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More clearances from Pain Relief Technologies
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