FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

INCARE PINSITE DRESSING

K Number: K905206 · Decision Apr 12, 1991
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
21
Applicant Total
85
Review Days
143

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Basic Information

Device Name
INCARE PINSITE DRESSING
K Number
K905206
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4018
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Hollister, Inc.
Date Received
November 20, 1990
Decision Date
April 12, 1991
Product Code
KOZ
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
KOZ Beads, Hydrophilic, For Wound Exudate Absorption

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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
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. →