# Accelerated Care Plus

- Location (FDA's records): Reno, NV
- FDA decisions: 3 (2006–2016): 3 510(k) clearances
- Names in FDA's records: Accelerated Care Plus (2); Accelerated Care Plus Corp. (1)
- Product codes: IMJ (1), KPI (1), ILY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K153456: Megapulse III Shortwave Diathermy (Jun 14, 2016)
- K093600: Omnistim Continence+ Pelvic Floor Stimulation System (Dec 4, 2009)
- K060191: Acp Omnipad Light Therapy System  & Acp Omnipad 500 Control Unit (Jul 12, 2006)

Source page: https://510kreport.com/company/accelerated-care-plus