Liquichek 182
Liquichek 182 is a Class I device made by Bio-Rad Laboratories, cleared under FDA 510(k) K050537 on 27 Apr 2005 and listed in FDA GUDID since 9 Jan 2017 (UDI-DI 00847661000631), 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 | Number00847661000631 | Date9 Jan 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK050537 | Date27 Apr 2005 | StatusActive |
Official records
- AccessGUDID record 00847661000631
- FDA 510(k) database K050537
Across registries
- FDA 510(k) K050537 decided 27 Apr 2005 Active
- FDA GUDID UDI-DI 00847661000631 listed 9 Jan 2017 Listed
Timeline
- Cleared FDA 510(k) K050537
- Listed FDA GUDID 00847661000631
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Liquichek
- Generic name
- Angiotensin converting enzyme (ACE) IVD, control
- Model / Ref / Catalog
- 182
- Primary DI / UDI-DI
- 00847661000631
- 510(k) Number
- FDA product code
- JJY
- GMDN term
- Angiotensin converting enzyme (ACE) IVD, control
- Device class
- Class I
- Regulation number
- 862.1660
- GUDID distribution status
- In Commercial Distribution
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