9007 L
by Medtronic PS Medical 2 variants
9007 L is a Class II device made by Medtronic PS Medical, cleared under FDA 510(k) K871752 on 22 May 1987 and listed in FDA GUDID since 30 Jun 2015 (UDI-DI 00673978249117), 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 | Number00673978249117 | Date30 Jun 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK871752 | Date22 May 1987 | StatusActive |
Official records
- AccessGUDID record 00673978249117
- FDA 510(k) database K871752
Across registries
- FDA 510(k) K871752 decided 22 May 1987 Active
- FDA GUDID UDI-DI 00673978249117 listed 30 Jun 2015 Listed
Timeline
- Cleared FDA 510(k) K871752
- Listed FDA GUDID 00673978249117
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Generic name
- Peritoneal/atrial cerebrospinal fluid catheter
- Model / reference
- 9007 L
- Primary DI / UDI-DI
- 00673978249117
- 510(k) Number
- FDA product code
- JXG
- GMDN term
- Peritoneal/atrial cerebrospinal fluid catheter
- Device class
- Class II
- Regulation number
- 882.5550
- GUDID distribution status
- In Commercial Distribution
- Size
- Outer Diameter — 2.5 MillimeterLength — 90.0 Centimeter
Similar devices in this category
Other devices filed under Peritoneal/atrial cerebrospinal fluid catheter.