ARP Rx100
ARP Rx100 is a Class II device made by Arp Manufacturing, Inc., cleared under FDA 510(k) K093259 on 17 Dec 2009 and listed in FDA GUDID since 23 Aug 2016 (UDI-DI M7570010320), active as of 31 May 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberM7570010320 | Date23 Aug 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK093259 | Date17 Dec 2009 | StatusActive |
Official records
- FDA 510(k) database K093259
Across registries
- FDA 510(k) K093259 decided 17 Dec 2009 Active
- FDA GUDID UDI-DI M7570010320 listed 23 Aug 2016 Listed
Timeline
- Cleared FDA 510(k) K093259
- Listed FDA GUDID M7570010320
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Generic name
- Physical therapy transcutaneous electrical stimulation system, line-powered
- Model / reference
- Rx100
- Primary DI / UDI-DI
- M7570010320
- 510(k) Number
- FDA product code
- IPF
- GMDN term
- Physical therapy transcutaneous electrical stimulation system, line-powered
- Device class
- Class II
- Regulation number
- 890.5850
- GUDID distribution status
- In Commercial Distribution
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