PainKARE— 510(k) K151034
Substantially EquivalentTriowave Technologies
FDA 510(k) clearance K151034 for PainKARE, Substantially Equivalent on 2015-11-21. Applicant: Triowave Technologies. Device class: 2.
Clearance details
- Applicant
- Triowave 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
- Fremont, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.