510(k) K102958

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

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