OmniVersa Multi-Modality Therapy System and Omnistim FX2 Professional Therapy System— 510(k) K153559
Substantially EquivalentAccelerated Care Plus (Acp)
FDA 510(k) clearance K153559 for OmniVersa Multi-Modality Therapy System and Omnistim FX2 Professional Therapy System, Substantially Equivalent on 2016-08-26. Applicant: Accelerated Care Plus (Acp). Device class: 2.
Clearance details
- Applicant
- Accelerated Care Plus (Acp)
- Product code
- Code IMG
- Device class
- Class 2
- Regulation
- 21 CFR 890.5860
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Reno, NV, US
Recent devices under product code IMG
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