Live View Panel (Lvp)
510(k) K131415
Live View Panel (Lvp) is a Class II device made by Neurotronics, Inc., cleared under FDA 510(k) K131415 on 9 Aug 2013, 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 | FDA 510(k)SESE | NumberK131415 | Date9 Aug 2013 | StatusActive |
Official records
- FDA 510(k) database K131415
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- OLV
- Device class
- Class II
- Regulation
- 21 CFR Part 882.1400
- Advisory committee
- Neurology
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K131415
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 | |||
|---|---|---|---|---|
| Live View Panel Pro Version 2.0 | 2.0 | 00817111021264 | — | On the market |
| Live View Panel Version 1.3 | 1.3 | 00817111020786 | — | No longer on the market |
| Live View Panel Version 1.4 | 1.4 | 00817111020816 | — | On the market |
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