510(k) K190270
K190270 is an FDA 510(k) premarket notification submitted by Cas Medical Systems, Inc. for the device "FORE-SIGHT ELITE Tissue Oximeter Module". The FDA issued a decision of Substantially Equivalent on Oct 21, 2019. The device falls under product code MUD (Oximeter, Tissue Saturation), a Class II device regulated under 21 CFR 870.2700. Cas Medical Systems, Inc. has 31 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 21, 2019
- Date Received
- Feb 8, 2019
- 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)