GENESIS(R) HOME UTERINE ACTIVITY MONITORING SYSTEM

FDA Premarket Approval P890063

This medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original pma or panel track supplement and may not represent the most recent labeling.

Pre-market Approval Supplement Details

DeviceGENESIS(R) HOME UTERINE ACTIVITY MONITORING SYSTEM
Generic NameMonitor, Uterine Contraction, External (for Use In Clinic)
ApplicantMATRIA HEALTHCARE, INC.
Date Received1989-11-15
Decision Date1990-09-12
Notice Date1990-10-23
PMAP890063
SupplementS
Product CodeHFM 
Docket Number90M-0315
Advisory CommitteeObstetrics/Gynecology
Expedited ReviewNo
Combination Product No
Applicant Address MATRIA HEALTHCARE, INC. 1850 Parkway Place suite 1200 marietta, GA 30067

Supplemental Filings

Supplement NumberDateSupplement Type
P890063Original Filing
S004 1993-04-07 Normal 180 Day Track
S003 1991-06-11 Normal 180 Day Track
S002 1990-12-21 Normal 180 Day Track
S001

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