ProHT JPD-FR401
ProHT JPD-FR401 is a Class II device made by Inland Products, Inc., cleared under FDA 510(k) K131243 on 12 Nov 2013 and listed in FDA GUDID since 16 Aug 2016 (UDI-DI 00012405890018), 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 | Number00012405890018 | Date16 Aug 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK131243 | Date12 Nov 2013 | StatusActive |
Official records
- AccessGUDID record 00012405890018
- FDA 510(k) database K131243
Across registries
- FDA 510(k) K131243 decided 12 Nov 2013 Active
- FDA GUDID UDI-DI 00012405890018 listed 16 Aug 2016 Listed
Timeline
- Cleared FDA 510(k) K131243
- Listed FDA GUDID 00012405890018
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- ProHT
- Generic name
- Infrared patient thermometer, ear
- Model / reference
- JPD-FR401
- Primary DI / UDI-DI
- 00012405890018
- 510(k) Number
- FDA product code
- FLL
- GMDN term
- Infrared patient thermometer, ear
- Device class
- Class II
- Regulation number
- 880.2910
- GUDID distribution status
- In Commercial Distribution
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