FDA 510(k) FDA unclassified Unknown 🇺🇸 United States

SIMPLICARE THIN FILM WOUND DRESSINGS

K Number: K980209 · Decision Feb 20, 1998
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
79
Applicant Total
85
Review Days
31

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SIMPLICARE THIN FILM WOUND DRESSINGS
K Number
K980209
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Unknown
Statement or Summary
Summary
Applicant
Hollister, Inc.
Date Received
January 20, 1998
Decision Date
February 20, 1998
Product Code
MGP
Advisory Committee
Unknown
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
MGP Dressing, Wound And Burn, Occlusive

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MGP), 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. →