510(k) K102958

PHILIPS AVALON FETAL MONITOR by Philips Medizin Systeme Boblingen GmbH — Product Code HGM

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