Papette 892030
by Andwin Scientific 2 variants
Papette (892030-P25) is a cervical cytology brush (FDA Class II; FDA product code HHT, Spatula, Cervical, Cytological) made by Andwin Scientific, cleared under FDA 510(k) K983428 on 16 Nov 1998 and listed in FDA GUDID since 1 Nov 2017 (UDI-DI 00187207000252), 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 | Number00187207000252 | Date1 Nov 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK983428 | Date16 Nov 1998 | StatusActive |
Official records
- AccessGUDID record 00187207000252
- FDA 510(k) database K983428
Across registries
- FDA 510(k) K983428 decided 16 Nov 1998 Active
- FDA GUDID UDI-DI 00187207000252 listed 1 Nov 2017 Listed
Timeline
- Cleared FDA 510(k) K983428
- Listed FDA GUDID 00187207000252
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Papette
- Generic name
- Cervical cytology brush
- Model / Ref / Catalog
- 892030, 892030-P25
- Primary DI / UDI-DI
- 00187207000252
- 510(k) Number
- FDA product code
- HHT
- GMDN term
- Cervical cytology brush
- Device class
- Class II
- Regulation number
- 884.4530
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Cervical cytology brush.