Stat Profile Prime Abg
by Nova Biomedical Corporation 5 variants
Stat Profile Prime Abg (53108) is a Class I device made by Nova Biomedical Corporation, cleared under FDA 510(k) K151982 on 10 Sep 2015 and listed in FDA GUDID since 20 Sep 2016 (UDI-DI 00385480531085), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None ongoingDocuments
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00385480531085 | Date20 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK151982 | Date10 Sep 2015 | StatusActive |
Official records
- AccessGUDID record 00385480531085
- FDA 510(k) database K151982
Across registries
- FDA 510(k) K151982 decided 10 Sep 2015 Active
- FDA GUDID UDI-DI 00385480531085 listed 20 Sep 2016 Listed
Recalls
-
- Terminated Z-2732-2017
Software- scheduled A-QC analysis could initiate prior to a patient result being released by the operator and result in the pending patient result being overwritten with the A-QC test results.
Timeline
- Cleared FDA 510(k) K151982
- Listed FDA GUDID 00385480531085
- Recall initiated FDA recalls Z-2732-2017
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Stat Profile
- Generic name
- Multiple blood gas/haemoximetry/electrolyte analyte IVD, control
- Model / Ref / Catalog
- PRIME ABG, 53108
- Primary DI / UDI-DI
- 00385480531085
- 510(k) Number
- FDA product code
- JJY
- GMDN term
- Multiple blood gas/haemoximetry/electrolyte analyte IVD, control
- Device class
- Class I
- Regulation number
- 862.1660
- GUDID distribution status
- In Commercial Distribution
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