Lyphochek 400
Lyphochek 400 is a multiple heavy metal IVD (FDA Class I; FDA product code DIE, Heavy Metals Control Materials) made by Bio-Rad Laboratories, cleared under FDA 510(k) K990928 on 16 Apr 1999 and listed in FDA GUDID since 9 Jan 2017 (UDI-DI 00847661000280), 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 | Number00847661000280 | Date9 Jan 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK990928 | Date16 Apr 1999 | StatusActive |
Official records
- AccessGUDID record 00847661000280
- FDA 510(k) database K990928
Across registries
- FDA 510(k) K990928 decided 16 Apr 1999 Active
- FDA GUDID UDI-DI 00847661000280 listed 9 Jan 2017 Listed
Timeline
- Cleared FDA 510(k) K990928
- Listed FDA GUDID 00847661000280
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Lyphochek
- Generic name
- Multiple heavy metal IVD, control
- Model / Ref / Catalog
- 400
- Primary DI / UDI-DI
- 00847661000280
- 510(k) Number
- FDA product code
- DIE
- GMDN term
- Multiple heavy metal IVD, control
- Device class
- Class I
- Regulation number
- 862.3280
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code DIE (HEAVY METALS CONTROL MATERIALS).