CRYOcheck™ Abnormal 1 Reference Control ARP1-05
CRYOcheck™ Abnormal 1 Reference Control ARP1-05 is a Class II device made by Precision Biologic, cleared under FDA 510(k) K952624 on 30 Oct 1995 and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00843876000077), 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 | Number00843876000077 | Date23 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK952624 | Date30 Oct 1995 | StatusActive |
Official records
- AccessGUDID record 00843876000077
- FDA 510(k) database K952624
Across registries
- FDA 510(k) K952624 decided 30 Oct 1995 Active
- FDA GUDID UDI-DI 00843876000077 listed 23 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K952624
- Listed FDA GUDID 00843876000077
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- CRYOcheck™ Abnormal 1 Reference Control
- Generic name
- Multiple coagulation marker IVD, control
- Model / reference
- ARP1-05
- Primary DI / UDI-DI
- 00843876000077
- 510(k) Number
- FDA product code
- GGN, GGC
- GMDN term
- Multiple coagulation marker IVD, control
- Device class
- Class II
- Regulation number
- 864.5425
- GUDID distribution status
- In Commercial Distribution
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