510(k) K102958
K102958 is an FDA 510(k) premarket notification submitted by Philips Medizin Systeme Boblingen GmbH for the device "PHILIPS AVALON FETAL MONITOR". The FDA issued a decision of Substantially Equivalent on March 18, 2011. The device falls under product code HGM (System, Monitoring, Perinatal), a Class II device regulated under 21 CFR 884.2740. Philips Medizin Systeme Boblingen GmbH has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 18, 2011
- Date Received
- October 4, 2010
- 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