Sensoronics SECG-PHP3L-1671
Sensoronics SECG-PHP3L-1671 is a Class II device made by Sensoronics Incorporated, cleared under FDA 510(k) K120010 on 19 Jan 2012 and listed in FDA GUDID since 26 Sep 2016 (UDI-DI 00851456007583), 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 | Number00851456007583 | Date26 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK120010 | Date19 Jan 2012 | StatusActive |
Official records
- AccessGUDID record 00851456007583
- FDA 510(k) database K120010
Across registries
- FDA 510(k) K120010 decided 19 Jan 2012 Active
- FDA GUDID UDI-DI 00851456007583 listed 26 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K120010
- Listed FDA GUDID 00851456007583
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Sensoronics
- Generic name
- Electrocardiographic lead set, reusable
- Model / reference
- SECG-PHP3L-1671
- Primary DI / UDI-DI
- 00851456007583
- 510(k) Number
- FDA product code
- DSA
- GMDN term
- Electrocardiographic lead set, reusable
- Device class
- Class II
- Regulation number
- 870.2900
- GUDID distribution status
- In Commercial Distribution
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