NvisionVLE Low-profile Optical Probe— 510(k) K191117
UnknownNinepoint Medical, Inc.
FDA 510(k) clearance K191117 for NvisionVLE Low-profile Optical Probe, Unknown on 2019-07-19. Applicant: Ninepoint Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Ninepoint Medical, Inc.
- Product code
- Code NQQ
- Device class
- Class 2
- Regulation
- 21 CFR 892.1560
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Bedford, MA, US
Recent devices under product code NQQ
view allMore clearances from Ninepoint Medical, Inc.
view all- K182616 — NvisionVLE Imaging System, NvisionVLE Optical Probe, NvisionVLE Inflation System
- K182261 — NvisionVLE Imaging System, NvisionVLE Optical Probe
- K153479 — NvisionVLE Imaging Console, NvisionVLE Marking Probe, 20mm balloon, NvisionVLE Marking Probe, 17mm balloon,NvisionVLE Marking Probe, 14mm balloon, NvisionVLE Inflation System
- K143678 — NvisionVLE Imaging System, NvisionVLE Optical Probe, NvisionVLE Inflation Accessory
- K120800 — NVISION VLE IMAGING SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.