PainAway Pro RTLAGF-900
PainAway Pro RTLAGF-900, a transcutaneous electrical stimulation electrode (FDA Class II) made by Drive Devilbiss Healthcare, was cleared under FDA 510(k) K102598 on 13 May 2011 and listed in FDA GUDID on 1 Jul 2016 (UDI-DI 00822383543727); the registry lists it as not in commercial distribution (GUDID) as of 23 Oct 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 | Number00822383543727 | Date1 Jul 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK102598 | Date13 May 2011 | StatusActive |
Official records
- AccessGUDID record 00822383543727
- FDA 510(k) database K102598
Across registries
- FDA 510(k) K102598 decided 13 May 2011 Active
- FDA GUDID UDI-DI 00822383543727 listed 1 Jul 2016 Listed
Timeline
- Cleared FDA 510(k) K102598
- Listed FDA GUDID 00822383543727
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- PainAway Pro
- Generic name
- Transcutaneous electrical stimulation electrode, single-use
- Model / reference
- RTLAGF-900
- Primary DI / UDI-DI
- 00822383543727
- 510(k) Number
- FDA product code
- NUH, NGX
- GMDN term
- Transcutaneous electrical stimulation electrode, single-use
- Device class
- Class II
- Regulation number
- 882.5890, 890.5850
- GUDID distribution status
- Not in Commercial Distribution
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