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

SUTURE REMOVAL KIT

K Number: K855131 · Decision Jan 13, 1986
Classifications
1
FEI Numbers
158
Registration Numbers
158
Same Product Code
6
Applicant Total
19
Review Days
21

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Basic Information

Device Name
SUTURE REMOVAL KIT
K Number
K855131
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6820
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Dynarex Corp.
Date Received
December 23, 1985
Decision Date
January 13, 1986
Product Code
JOK
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JOK Scissors, Medical, Disposable

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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. →