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EKD — Instrument, Cutting, Operative Class I

FDA Device Classification

FDA product code EKD covers "Instrument, Cutting, Operative", a Class I medical device regulated under 21 CFR 872.4565. Submissions are reviewed by the Dental panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

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

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K851723artiberia1300/10 TO 1305/89-92 VARIOUS CUTTING INSTRUMENTSJuly 2, 1985
K821790pacific dentalBEACH EXCAVATOR'S NO. 1 & NO. 2July 6, 1982

FDA data resources