Selectiva 1808004A
by Heraeus Medical Components LLC 2 variants
Selectiva 1808004A is a Class II device made by Heraeus Medical Components LLC, cleared under FDA 510(k) K013024 on 4 Dec 2001 and listed in FDA GUDID since 21 Sep 2016 (UDI-DI 00857834006636), 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 | Number00857834006636 | Date21 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK013024 | Date4 Dec 2001 | StatusActive |
Official records
- AccessGUDID record 00857834006636
- FDA 510(k) database K013024
Across registries
- FDA 510(k) K013024 decided 4 Dec 2001 Active
- FDA GUDID UDI-DI 00857834006636 listed 21 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K013024
- Listed FDA GUDID 00857834006636
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Selectiva
- Generic name
- Peripheral vascular guidewire, manual
- Model / reference
- 1808004A
- Primary DI / UDI-DI
- 00857834006636
- 510(k) Number
- FDA product code
- DQX
- GMDN term
- Peripheral vascular guidewire, manual
- Device class
- Class II
- Regulation number
- 870.1330
- GUDID distribution status
- In Commercial Distribution
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