JAS Diagnostics DG-GLO2-125
JAS Diagnostics DG-GLO2-125 is a Class II device made by Drew Scientific, Ltd., cleared under FDA 510(k) K970781 on 21 Apr 1997 and listed in FDA GUDID since 9 Sep 2016 (UDI-DI 00817274021613), 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 | Number00817274021613 | Date9 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK970781 | Date21 Apr 1997 | StatusActive |
Official records
- AccessGUDID record 00817274021613
- FDA 510(k) database K970781
Across registries
- FDA 510(k) K970781 decided 21 Apr 1997 Active
- FDA GUDID UDI-DI 00817274021613 listed 9 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K970781
- Listed FDA GUDID 00817274021613
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- JAS Diagnostics
- Generic name
- Glucose/ketone/lipid profile IVD, kit, enzyme spectrophotometry
- Model / reference
- DG-GLO2-125
- Primary DI / UDI-DI
- 00817274021613
- 510(k) Number
- FDA product code
- CGA
- GMDN term
- Glucose/ketone/lipid profile IVD, kit, enzyme spectrophotometry
- Device class
- Class II
- Regulation number
- 862.1345
- GUDID distribution status
- In Commercial Distribution
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