Ready Sensor™ Glucose Biosensor 10312818
by Siemens Healthcare Diagnostics Inc.
Ready Sensor™ Glucose Biosensor 10312818 (570024) is a Class II device made by Siemens Healthcare Diagnostics Inc., cleared under FDA 510(k) K934907 on 3 Jan 1994 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00630414121154), 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 | Number00630414121154 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK934907 | Date3 Jan 1994 | StatusActive |
Official records
- AccessGUDID record 00630414121154
- FDA 510(k) database K934907
Across registries
- FDA 510(k) K934907 decided 3 Jan 1994 Active
- FDA GUDID UDI-DI 00630414121154 listed 24 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K934907
- Listed FDA GUDID 00630414121154
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Ready Sensor™ Glucose Biosensor
- Generic name
- Glucose IVD, kit, ion-selective electrode (ISE)
- Model / Ref / Catalog
- 10312818, 570024
- Primary DI / UDI-DI
- 00630414121154
- 510(k) Number
- FDA product code
- CHL
- GMDN term
- Glucose IVD, kit, ion-selective electrode (ISE)
- Device class
- Class II
- Regulation number
- 862.1120
- GUDID distribution status
- In Commercial Distribution
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