Micro-X K100-0105
Micro-X K100-0105 is a Class II device made by Reprocessing Products Corp, cleared under FDA 510(k) K974426 on 10 Feb 1999 and listed in FDA GUDID since 7 Mar 2017 (UDI-DI 00858293006120), active as of 22 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 | Number00858293006120 | Date7 Mar 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK974426 | Date10 Feb 1999 | StatusActive |
Official records
- AccessGUDID record 00858293006120
- FDA 510(k) database K974426
Across registries
- FDA 510(k) K974426 decided 10 Feb 1999 Active
- FDA GUDID UDI-DI 00858293006120 listed 7 Mar 2017 Listed
Timeline
- Cleared FDA 510(k) K974426
- Listed FDA GUDID 00858293006120
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Micro-X
- Generic name
- Medical device disinfection solution test strip
- Model / Ref / Catalog
- K100-0105
- Primary DI / UDI-DI
- 00858293006120
- 510(k) Number
- FDA product code
- LIF
- GMDN term
- Medical device disinfection solution test strip
- Device class
- Class II
- Regulation number
- 876.5820
- GUDID distribution status
- In Commercial Distribution