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EKQ — Preparer, Root Canal Endodontic Class I

FDA Device Classification

FDA product code EKQ covers "Preparer, Root Canal Endodontic", 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
EKQ
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
K832378syntex dental productsVIBRATORY ENDODONTIC SYSTEMOctober 4, 1983
K801463almore intlOJ-1 ENDODONIC ROOT CANAL FILE HOLDERJuly 21, 1980

FDA data resources