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EKB — Explorer, Operative Class I

FDA Device Classification

FDA product code EKB covers "Explorer, Operative", a Class I medical device regulated under 21 CFR 872.4565. Submissions are reviewed by the Dental panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
EKB
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
K851724artiberia1410/1 TO 1435/13 VARIOUS PROBES & EXPLORERSJuly 2, 1985
K823914treace medicalEXPLORER TIPJanuary 21, 1983
K821780pacific dentalBEACH EXPLORER NO. 23T.G.July 6, 1982

FDA data resources