Cherish Serenity CS1245
Cherish Serenity CS1245 is a Class II device made by LifeSignals, Inc., cleared under FDA 510(k) K172011 on 14 Jun 2018 and listed in FDA GUDID since 20 May 2020 (UDI-DI B353CS124501), active (FDA 510(k)), not in commercial distribution (GUDID) 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 | NumberB353CS124501 | Date20 May 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK172011 | Date14 Jun 2018 | StatusActive |
Official records
- FDA 510(k) database K172011
Across registries
- FDA 510(k) K172011 decided 14 Jun 2018 Active
- FDA GUDID UDI-DI B353CS124501 listed 20 May 2020 Listed
Timeline
- Cleared FDA 510(k) K172011
- Listed FDA GUDID B353CS124501
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Cherish Serenity
- Generic name
- Electrocardiography telemetric monitoring system
- Model / reference
- CS1245
- Primary DI / UDI-DI
- B353CS124501
- 510(k) Number
- FDA product code
- DRT, DRG, DRX
- GMDN term
- Electrocardiography telemetric monitoring system
- Device class
- Class II
- Regulation number
- 870.2300, 870.2910, 870.2360
- GUDID distribution status
- Not in Commercial Distribution
- MRI safety
- MR Unsafe
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