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

DYNAREX GAUZE SPONGE OR PADS

K Number: K933308 · Decision Dec 22, 1993
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
270
Applicant Total
19
Review Days
168

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Basic Information

Device Name
DYNAREX GAUZE SPONGE OR PADS
K Number
K933308
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Dynarex Corp.
Date Received
July 7, 1993
Decision Date
December 22, 1993
Product Code
EFQ
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
EFQ Gauze/Sponge, Internal

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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
K991695 DYNAREX NON-WOVEN SPONGE
K991694 DYNAREX DRAIN SPONGE
K983348 DYNAREX TRACHEOSTOMY SPONGE
K960388 DYNAREX NON-WOVEN SPONGE
K951660 DYNAREX GAUZE SPONGE
Search all 19 clearances from Dynarex Corp. →