TLC Diagnostics TLC 1-Stop Alert
by Datrix LLC
TLC Diagnostics TLC 1-Stop Alert (RX93030-013) is a Class II device made by Datrix LLC, cleared under FDA 510(k) K112601 on 9 Nov 2011 and listed in FDA GUDID since 29 May 2019 (UDI-DI 00851074007392), 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 | Number00851074007392 | Date29 May 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK112601 | Date9 Nov 2011 | StatusActive |
Official records
- AccessGUDID record 00851074007392
- FDA 510(k) database K112601
Across registries
- FDA 510(k) K112601 decided 9 Nov 2011 Active
- FDA GUDID UDI-DI 00851074007392 listed 29 May 2019 Listed
Timeline
- Cleared FDA 510(k) K112601
- Listed FDA GUDID 00851074007392
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- TLC Diagnostics
- Generic name
- Telemetric electrocardiographic ambulatory recorder
- Model / Ref / Catalog
- TLC 1-Stop Alert, RX93030-013
- Primary DI / UDI-DI
- 00851074007392
- 510(k) Number
- FDA product code
- MWJ
- GMDN term
- Telemetric electrocardiographic ambulatory recorder
- Device class
- Class II
- Regulation number
- 870.2800
- GUDID distribution status
- In Commercial Distribution
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