Indiba Activ - Activ 902 ACT229
by Indiba SA.
Indiba Activ - Activ 902 ACT229 is a medium-wave diathermy treatment system (FDA Class II; FDA product code PBX, Massager, vacuum, radio frequency induced heat) made by Indiba SA., cleared under FDA 510(k) K161458 on 3 Oct 2016 and listed in FDA GUDID since 22 Feb 2019 (UDI-DI 08434251000014), active 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 | Number08434251000014 | Date22 Feb 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK161458 | Date3 Oct 2016 | StatusActive |
Official records
- AccessGUDID record 08434251000014
- FDA 510(k) database K161458
Across registries
- FDA 510(k) K161458 decided 3 Oct 2016 Active
- FDA GUDID UDI-DI 08434251000014 listed 22 Feb 2019 Listed
Timeline
- Cleared FDA 510(k) K161458
- Listed FDA GUDID 08434251000014
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Indiba Activ - Activ 902
- Generic name
- Medium-wave diathermy treatment system
- Model / Ref / Catalog
- ACT229
- Primary DI / UDI-DI
- 08434251000014
- 510(k) Number
- FDA product code
- PBX
- GMDN term
- Medium-wave diathermy treatment system
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
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