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

HOLLISTER HORIZONTAL DRAIN/TUBE ATTACHMENT DEVICE

K Number: K922739 · Decision Aug 6, 1992
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
76
Applicant Total
85
Review Days
59

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Basic Information

Device Name
HOLLISTER HORIZONTAL DRAIN/TUBE ATTACHMENT DEVICE
K Number
K922739
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hollister, Inc.
Date Received
June 8, 1992
Decision Date
August 6, 1992
Product Code
GBX
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
GBX Catheter, Irrigation

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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. →