510(k) K254036
K254036 is an FDA 510(k) premarket notification submitted by Datex Ohmeda, Inc. for the device "Novii+ Wireless Patch System". The FDA issued a decision of Substantially Equivalent on August 10, 2026. The device falls under product code HGM (System, Monitoring, Perinatal), a Class II device regulated under 21 CFR 884.2740. Datex Ohmeda, Inc. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 10, 2026
- Date Received
- December 16, 2025
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Monitoring, Perinatal
- Device Class
- Class II
- Regulation Number
- 884.2740
- Review Panel
- OB
- Submission Type