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

DYNAREX NON-WOVEN SPONGE

K Number: K991695 · Decision Jul 15, 1999
Classifications
1
FEI Numbers
79
Registration Numbers
79
Same Product Code
221
Applicant Total
19
Review Days
58

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Basic Information

Device Name
DYNAREX NON-WOVEN SPONGE
K Number
K991695
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5090
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Dynarex Corp.
Date Received
May 18, 1999
Decision Date
July 15, 1999
Product Code
KMF
Advisory Committee
General Hospital
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
KMF Bandage, Liquid

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Other Clearances by Dynarex Corp.

K Number Device Name
K052743 DYNAREX CPR SHIELD WITH ONE WAY VALVE AND BARRIER FILTER, MODEL 4921
K052314 DYNAREX VAGINAL SPECULA 4900, MODELS 4911-SMALL, 4912-MEDIUM, 4913-LARGE
K012816 DYNAREX IODOFORM PACKING STRIPS, MODELS 3411, 3412, 3413, 3414
K012957 TOWEL DRAPE, MODELS 4409, 4410
K012917 DYNAREX UMBILICAL CORD LAMP, MODELS 6833 AND 6833-B
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. →