RELIANCE URINARY CONTROL INSERT AND SIZING DEVICE

FDA Premarket Approval P960020

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

Approval for the reliance urinary control insert and sizing device

DeviceRELIANCE URINARY CONTROL INSERT AND SIZING DEVICE
Generic NameTransurethral Occlusion Insert, Urinary Incontinence-control, Female
ApplicantUROMED CORP.
Date Received1995-08-18
Decision Date1996-08-16
Notice Date1996-12-02
PMAP960020
SupplementS
Product CodeOCK 
Docket Number96M-0447
Advisory CommitteeGastroenterology/Urology
Expedited ReviewYes
Combination Product No
Applicant Address UROMED CORP. 64 A St. needham, MA 02194

Supplemental Filings

Supplement NumberDateSupplement Type
P960020Original Filing
S001 1999-03-17 Normal 180 Day Track

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