Vantage View System
510(k) K110085
Vantage View System is a Class II device made by St Jude Medical, cleared under FDA 510(k) K110085 on 26 Jan 2011, active as of 11 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK110085 | Date26 Jan 2011 | StatusActive |
Official records
- FDA 510(k) database K110085
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- DXJ
- Device class
- Class II
- Regulation
- 21 CFR Part 870.2450
- Advisory committee
- Cardiovascular
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K110085
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| VantageView™ H700470 | H700470 / H700470 | 05415067004703 | On the market | |
| VantageView™ System | A2184201 / System | 05414734218429 | On the market | |
| VantageView™ System | A21843 / System | 05414734218436 | On the market | |
| VantageView™ System | H700584 / System | 05415067005847 | On the market | |
| VantageView™ System | H701461 / System | 05415067014610 | On the market | |
| VantageView™ System | H701462 / System | 05415067014627 | On the market | |
| VantageView™ System | VS100001 / System | 05414734218412 | On the market | |
| VantageView™ System | VS100004 / System | 05415067010858 | On the market | |
| VantageView™ System | VS100005 / System | 05415067010865 | On the market | |
| VantageView™ VS100003 | VS100003 / VS100003 | 05415067010841 | On the market | |
| VantageView™ VS100006 | VS100006 / VS100006 | 05415067010872 | On the market | |
| WorkMate Claris™ H701312 | H701312 / H701312 | 05415067013125 | On the market | |
| WorkMate Claris™ H701313 | H701313 / H701313 | 05415067013132 | On the market |
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Other devices filed under FDA product code DXJ (Display, Cathode-Ray Tube, Medical).
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- CENTRALSCOPE 12 by Marquette Electronics, Inc.