Atlas FDA

FEMSOFT URETHRAL INSERT

FDA premarket approval P990002 · decided 1999-09-30

Approval details

PMA number
P990002
Trade name
FEMSOFT URETHRAL INSERT
Generic name
Transurethral occlusion insert, urinary incontinence-control, female
Applicant
Rochester Medical Corp.
Date received
1999-01-19
Decision date
1999-09-30
Days to decision
254 days
Decision code
APWD
Product code
OCK
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Stewartville, MN
Statement
The device is indicated for the management of stress urinary incontinence in adult females.

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510(k) clearances by this applicant

RecordFirmDate
HYDROSIL; MAGIC; PERSONAL CATHETER (K122785)Rochester Medical Corp.2013-05-14
HYDROPHILIC-ANTIBACTERIAL INTERMITTENT CATHETER, INTERMITTENT CATHETER CLOSED SYSTEM KIT (K033477)Rochester Medical Corp.2004-06-10
RELEASE NF ANTIBACTERIAL FOLEY CATHETER, ANTIBACTERIAL PERSONAL CATHETER (K001143)Rochester Medical Corp.2000-07-07
HYDROPHILIC SILICONE FOLEY CATHETER AND PERSONAL CATHETER (HYDROPHILIC AND NON-HYDROPHILIC) (K000723)Rochester Medical Corp.2000-05-19
ALL SILICONE FOLEY CATHETER, TWO-WAY FOLEY CATHETER, THREE-WAY FOLEY CATHETER, TWO-WAY RADIOPAQUE FOLEY CATHETER (K981612)Rochester Medical Corp.1998-07-08
SILICONE ANTIBACTERIAL FOLEY CATHETER (K971627)Rochester Medical Corp.1998-01-13
PERSONAL CATHETER (K970704)Rochester Medical Corp.1997-03-13
ROCHESTER MEDICAL CORPORATION SILICONE MALE EXTERNAL CATHETER (K952082)Rochester Medical Corp.1995-07-18