FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

DYNAREX IODOFORM PACKING STRIPS, MODELS 3411, 3412, 3413, 3414

K Number: K012816 · Decision Oct 17, 2002
Classifications
1
FEI Numbers
384
Registration Numbers
385
Same Product Code
702
Applicant Total
19
Review Days
421

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Basic Information

Device Name
DYNAREX IODOFORM PACKING STRIPS, MODELS 3411, 3412, 3413, 3414
K Number
K012816
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dynarex Corp.
Date Received
August 22, 2001
Decision Date
October 17, 2002
Product Code
FRO
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
FRO Dressing, Wound, Drug

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K012957 TOWEL DRAPE, MODELS 4409, 4410
K012917 DYNAREX UMBILICAL CORD LAMP, MODELS 6833 AND 6833-B
K991695 DYNAREX NON-WOVEN SPONGE
K991694 DYNAREX DRAIN SPONGE
K983348 DYNAREX TRACHEOSTOMY SPONGE
K960388 DYNAREX NON-WOVEN SPONGE
K951660 DYNAREX GAUZE SPONGE
K933308 DYNAREX GAUZE SPONGE OR PADS
Search all 19 clearances from Dynarex Corp. →