GENESIS HOME UTERINE ACTIVITY MONITORING SYSTEM (HUAM)

FDA Premarket Approval P890063 S004

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

DeviceGENESIS HOME UTERINE ACTIVITY MONITORING SYSTEM (HUAM)
Generic NameMonitor, Uterine Contraction, External (for Use In Clinic)
ApplicantMATRIA HEALTHCARE, INC.
Date Received1993-04-07
Decision Date1995-06-16
PMAP890063
SupplementS004
Product CodeHFM 
Advisory CommitteeObstetrics/Gynecology
Supplement TypeNormal 180 Day Track
Supplement ReasonChange Design/components/specifications/material
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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