Selectiva 1806004S
by Heraeus Medical Components LLC
Selectiva 1806004S 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 00857834006575), 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 | Number00857834006575 | Date21 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK013024 | Date4 Dec 2001 | StatusActive |
Official records
- AccessGUDID record 00857834006575
- FDA 510(k) database K013024
Across registries
- FDA 510(k) K013024 decided 4 Dec 2001 Active
- FDA GUDID UDI-DI 00857834006575 listed 21 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K013024
- Listed FDA GUDID 00857834006575
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- Withdrawn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
- 1806004S
- Primary DI / UDI-DI
- 00857834006575
- 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
Similar devices in this category
Other devices filed under Peripheral vascular guidewire, manual.
- Cook G00426 THSF-38-145 by COOK INCORPORATED
- Amplatz G03565 THSCF-35-180-3-AES by COOK INCORPORATED
- SplashWire™ 00884450529461 MSWSTDA25260EX by Merit Medical Systems, Inc.
- Guidewire SGW-066-07 SW30-140 by GALT MEDICAL CORP.
- Guidewire SGW-011-20 by GALT MEDICAL CORP.
- SplashWire™ 00884450529447 MSWSTFA35260EX by Merit Medical Systems, Inc.
- Transend™ M001468120 by Boston Scientific
- Transend™ M001468100 by Boston Scientific
- Guidewire 0.018 4/270cm angled (Straub Medical®) Version 1.0 80234 by Straub Medical AG