510(k) K812256
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 20, 1981
- Date Received
- August 12, 1981
- 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