KYX — Dispenser, Liquid Medication Class I

FDA Device Classification

FDA product code KYX covers "Dispenser, Liquid Medication", a Class I medical device regulated under 21 CFR 880.6430. Submissions are reviewed by the General Hospital panel. At least 11 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
KYX
Device Class
Class I
Regulation Number
880.6430
Submission Type
Review Panel
HO
Medical Specialty
General Hospital
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K143177kleengelKleenGel DispenserSeptember 14, 2015
K980109sangstat medicalCYCLOTECH CYCLOSPORINE ORAL SOLUTIONS DISPENSERAugust 18, 1998
K954181canyon medical productsCANYONS BI-DIRECTIONAL CHECK VALVENovember 29, 1995
K830571burron medical productsBOTTLE ADAPTERMarch 24, 1983
K801008burron medical productsMULTI-AD FLUID DISPENSING PUMP MP-3000June 2, 1980
K800362pharmaseal laboratoriesFLUID DISPENSING SYSTEMMarch 12, 1980
K800437burron medical productsSYRINGE TIP CONNECTORMarch 12, 1980
K792227national patent developmentMULTI-AD FLUID DISPENSING SYSTEMDecember 20, 1979
K781364baxa corp., sub. of cook groupPINT BOTTLE WELLOctober 17, 1978
K771539tridakSTEPPEROctober 7, 1977
K760517landmark plasticsCUP, DISPOSABLE MEDICINENovember 12, 1976