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KBM — Dissector, Tonsil Class I

FDA Device Classification

Classification Details

Product Code
KBM
Device Class
Class I
Regulation Number
874.4420
Submission Type
Review Panel
EN
Medical Specialty
Ear, Nose, Throat
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K940903medical insightsTONSIL SPONGE, GAUZE DISSECTOR, CYLINDRICAL SPONGESApril 14, 1994