EEF — Clamp, Rubber Dam Class I

FDA Device Classification

FDA product code EEF covers "Clamp, Rubber Dam", a Class I medical device regulated under 21 CFR 872.6300. 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
EEF
Device Class
Class I
Regulation Number
872.6300
Submission Type
Review Panel
DE
Medical Specialty
Dental
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K071615sybron dental specialtiesFIXAFLOSSSeptember 21, 2007
K915207bay technical productsDISPOSABLE RADIOLUCENT RUBBER DAM CLAMPFebruary 14, 1992
K780744hygienic dental mfg., co., theBRINKER TISSUE RETRACTORSMay 12, 1978