FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

INCARE PELVIC FLOOR THERAPY SYSTEM WITH DESKTOP COMPUTER

K Number: K961872 · Decision Aug 9, 1996
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
87
Applicant Total
85
Review Days
86

Basic Information

Device Name
INCARE PELVIC FLOOR THERAPY SYSTEM WITH DESKTOP COMPUTER
K Number
K961872
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5320
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
HOLLISTER, INC.
Date Received
May 15, 1996
Decision Date
August 9, 1996
Product Code
KPI
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KPI Stimulator, Electrical, Non-Implantable, For Incontinence

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KPI), ordered by most recent decision date.

View all

Other Clearances by HOLLISTER, INC.

K Number Device Name
K123804 INSTAFLO BOWEL CATHETER SYSTEM KIT
K100273 INSTAFLO BOWEL CATHETER SYSTEM KIT
K090960 VAPRO INTERMITTENT CATHETER, MODEL 72062, 72082,72102, 72122, 72142, 72064, 72084, 72104, 72124,72144, 72164, 72184,
K083153 ACTIFLO INDWELLING BOWEL CATHETER SYSTEM KIT, MODELS: 32004, 32005, 32006, 32007
K050483 EVADRI BLADDER CONTROL SYSTEMS
K040779 RESTORE WOUND CLEANSER
K013612 INCARE PELVIC FLOOR THERAPY SYSTEM
K013653 INCARE PRESSURE BIOFEEDBACK VAGINAL PRESSURE PROBE AND ANAL PRESSURE PROBE
K013483 INCARE ADVANCE; INTERMITTENT CATHETER, PLUS INTERMITTENT CATHETER, PLUS KIT
K013345 INCARE INTERMITTENT CATHETER
Search all 85 clearances from HOLLISTER, INC. →