Good Neighbor 90-331
by Amerisourcebergen Drug Corporation
Good Neighbor 90-331 is a Class II device made by Amerisourcebergen Drug Corporation, cleared under FDA 510(k) K032362 on 4 Dec 2003 and listed in FDA GUDID since 26 Sep 2024 (UDI-DI 00087701429484), 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 | Number00087701429484 | Date26 Sep 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK032362 | Date4 Dec 2003 | StatusActive |
Official records
- AccessGUDID record 00087701429484
- FDA 510(k) database K032362
Across registries
- FDA 510(k) K032362 decided 4 Dec 2003 Active
- FDA GUDID UDI-DI 00087701429484 listed 26 Sep 2024 Listed
Timeline
- Cleared FDA 510(k) K032362
- Listed FDA GUDID 00087701429484
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Good Neighbor
- Generic name
- Infrared patient thermometer, skin
- Model / reference
- 90-331
- Primary DI / UDI-DI
- 00087701429484
- 510(k) Number
- FDA product code
- FLL
- GMDN term
- Infrared patient thermometer, skin
- Device class
- Class II
- Regulation number
- 880.2910
- GUDID distribution status
- In Commercial Distribution
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