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

INSTAFLO BOWEL CATHETER SYSTEM KIT

K Number: K123804 · Decision Apr 17, 2013
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
85
Review Days
128

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Basic Information

Device Name
INSTAFLO BOWEL CATHETER SYSTEM KIT
K Number
K123804
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hollister, Inc.
Date Received
December 10, 2012
Decision Date
April 17, 2013
Product Code
KNT
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
KNT Tubes, Gastrointestinal (And Accessories)

Similar 510(k) Clearances

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Other Clearances by Hollister, Inc.

K Number Device Name
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
K013141 MICROGYN PLUS STIMULATION DEVICE
Search all 85 clearances from Hollister, Inc. →