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

INCARE PELVIC FLOOR THERAPY SYSTEM

K Number: K013612 · Decision Mar 19, 2002
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
64
Applicant Total
85
Review Days
134

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Basic Information

Device Name
INCARE PELVIC FLOOR THERAPY SYSTEM
K Number
K013612
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1425
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hollister, Inc.
Date Received
November 5, 2001
Decision Date
March 19, 2002
Product Code
HIR
Advisory Committee
Obstetrics/Gynecology
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
HIR Perineometer

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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
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
K013141 MICROGYN PLUS STIMULATION DEVICE
Search all 85 clearances from Hollister, Inc. →