Moore Medical 63347
Moore Medical 63347 is a Class II device made by Moore Medical Corp., cleared under FDA 510(k) K940686 on 8 Jul 1994 and listed in FDA GUDID since 9 Dec 2016 (UDI-DI 20607415001192), 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 | Number20607415001192 | Date9 Dec 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK940686 | Date8 Jul 1994 | StatusActive |
Official records
- AccessGUDID record 20607415001192
- FDA 510(k) database K940686
Across registries
- FDA 510(k) K940686 decided 8 Jul 1994 Active
- FDA GUDID UDI-DI 20607415001192 listed 9 Dec 2016 Listed
Timeline
- Cleared FDA 510(k) K940686
- Listed FDA GUDID 20607415001192
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Moore Medical
- Generic name
- Intermittent electronic patient thermometer
- Model / reference
- 63347
- Primary DI / UDI-DI
- 20607415001192
- 510(k) Number
- FDA product code
- FLL
- GMDN term
- Intermittent electronic patient thermometer
- Device class
- Class II
- Regulation number
- 880.2910
- GUDID distribution status
- Not in Commercial Distribution
Similar devices in this category
Other devices filed under Intermittent electronic patient thermometer.