Rpc 7001-3902W
Rpc 7001-3902W is a Class II device made by Reprocessing Products Corp, cleared under FDA 510(k) K852605 on 29 Jul 1985 and listed in FDA GUDID since 19 Jan 2017 (UDI-DI 00858293006007), active as of 22 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 | Number00858293006007 | Date19 Jan 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK852605 | Date29 Jul 1985 | StatusActive |
Official records
- AccessGUDID record 00858293006007
- FDA 510(k) database K852605
Across registries
- FDA 510(k) K852605 decided 29 Jul 1985 Active
- FDA GUDID UDI-DI 00858293006007 listed 19 Jan 2017 Listed
Timeline
- Cleared FDA 510(k) K852605
- Listed FDA GUDID 00858293006007
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Rpc
- Generic name
- Haemodialysis blood tubing set, single-use
- Model / Ref / Catalog
- 7001-3902W
- Primary DI / UDI-DI
- 00858293006007
- 510(k) Number
- FDA product code
- FJK
- GMDN term
- Haemodialysis blood tubing set, single-use
- Device class
- Class II
- Regulation number
- 876.5820
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Haemodialysis blood tubing set, single-use.