OCK

Product Code: OCK


Products Classified as OCK

2220Transurethral Occlusion Insert, Urinary Incontinence-control, Female

Total Product Life Cycle (TPLC) Devices

2220Transurethral Occlusion Insert, Urinary Incontinence-control, Female

Pre-market Approvals for OCK

P990002FEMSOFT URETHRAL INSERTROCHESTER MEDICAL CORP.

Global Unique Device Identification Database

00801741011122Transurethral occlusion insert, urinary incontinence-control, female
10801741011112Transurethral occlusion insert, urinary incontinence-control, female
10801741011105Transurethral occlusion insert, urinary incontinence-control, female
10801741011099Transurethral occlusion insert, urinary incontinence-control, female
10801741011082Transurethral occlusion insert, urinary incontinence-control, female
10801741011075Transurethral occlusion insert, urinary incontinence-control, female
10801741011068Transurethral occlusion insert, urinary incontinence-control, female

Maude Adverse Events

FEMSOFT? INSERT FEMALE URETHRAL INSERTC.R. BARD, INC. (COVINGTON) -10182332018-04-09
FEMSOFTINSERTROCHESTER MEDICAL CORP.2015-02-20
FEM SOFTROCHESTER MEDICAL CORP2011-11-30
FEMSOFTROCHESTER MEDICAL CORP.2011-10-20
FEMSOFT INSERTROCHESTER MEDICAL CORP2010-06-29
FEMSOFT INSERTROCHESTER MEDICAL CORP.2010-05-13
FEMSOFT INSERTROCHESTER MEDICAL CORP.2010-05-13

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.