510(k) K821478
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 26, 1982
- Date Received
- May 18, 1982
- 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