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EMK — Curette, Surgical, Dental Class I

FDA Device Classification

Classification Details

Product Code: EMK
Device Class: Class I
Regulation Number: 872.4565
Submission Type
Review Panel: DE
Medical Specialty: Dental
Implant: No

Recent 510(k) Clearances

K-Number	Applicant	Device Name	Date
K851718	artiberia	930/0 TO 950/6 VARIOUS TYPES OF BONE CURETTES	July 2, 1985