V-Pvp
510(k) K232125
V-Pvp is a medical device (FDA Class II; FDA product code MQL, Media, Reproductive) made by VITROMED GmbH, cleared under FDA 510(k) K232125 on 20 Mar 2024, 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 | NumberK232125 | Date20 Mar 2024 | StatusActive |
Official records
- FDA 510(k) database K232125
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MQL
- Device class
- Class II
- Regulation
- 21 CFR Part 884.6180
- Advisory committee
- Obstetrics/Gynecology
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K232125
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 | |||
|---|---|---|---|---|
| V-PVP-7 | V-PVP-7 | 04260650071034 | — | On the market |
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