SonicLift— 510(k) K150077
Substantially EquivalentPretika Corporation
FDA 510(k) clearance K150077 for SonicLift, Substantially Equivalent on 2015-11-25. Applicant: Pretika Corporation. Device class: 2.
Clearance details
- Applicant
- Pretika Corporation
- Product code
- Code NFO
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Riverside, CA, US
Recent devices under product code NFO
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