510(k) K791035
K791035 is an FDA 510(k) premarket notification submitted by Roche Medical Electronics, Inc. for the device "FETASONDE FETAL ACTIVITY MONITOR". The FDA issued a decision of Substantially Equivalent on September 4, 1979. The device falls under product code HGM (System, Monitoring, Perinatal), a Class II device regulated under 21 CFR 884.2740. Roche Medical Electronics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 4, 1979
- Date Received
- June 5, 1979
- 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