510(k) K161237
K161237 is an FDA 510(k) premarket notification submitted by Hypermed Imaging, Inc. for the device "HyperView Hyperspectral Tissue Oxygenation Measurement System". The FDA issued a decision of Substantially Equivalent on Dec 16, 2016. The device falls under product code MUD (Oximeter, Tissue Saturation), a Class II device regulated under 21 CFR 870.2700.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 16, 2016
- Date Received
- May 2, 2016
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Oximeter, Tissue Saturation
- Device Class
- Class II
- Regulation Number
- 870.2700
- Review Panel
- SU
- Submission Type
- 510(k)