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EIF — Accessories, Retractor, Dental Class I

FDA Device Classification

FDA product code EIF covers "Accessories, Retractor, Dental", a Class I medical device regulated under 21 CFR 872.4565. Submissions are reviewed by the Dental panel. At least 4 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
EIF
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
K940785worldwide dentalMOUTH PROPSOctober 5, 1994
K873960cheri lewis, d.d.sLEWIS SAFE SLEEVEDecember 4, 1987
K830187hematology marketing assocFOCUS FLUIDMarch 1, 1983
K830116north pacific dentalSULCARINGSFebruary 18, 1983

FDA data resources