NvisionVLE Imaging System, NvisionVLE Optical Probe— 510(k) K182261

Unknown

Ninepoint Medical, Inc.

FDA 510(k) clearance K182261 for NvisionVLE Imaging System, NvisionVLE Optical Probe, Unknown on 2018-10-16. 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
Special
Location
Bedford, MA, US
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