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KYW — Container, Liquid Medication, Graduated Class I

FDA Device Classification

Classification Details

Product Code
KYW
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
K800213cutter laboratoriesPHARMACY ADDITIVE SYRINGE SETFebruary 26, 1980
K791345general clinical plasticsMEDICINE CUPAugust 3, 1979