FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

TRACHEOSTOMY CARE KIT

K Number: K855130 · Decision Mar 4, 1986
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
127
Applicant Total
19
Review Days
71

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Basic Information

Device Name
TRACHEOSTOMY CARE KIT
K Number
K855130
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5800
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Dynarex Corp.
Date Received
December 23, 1985
Decision Date
March 4, 1986
Product Code
BTO
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BTO Tube, Tracheostomy (W/Wo Connector)

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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. →