ELK — Teeth, Artificial, Backing And Facing Class I

FDA Device Classification

FDA product code ELK covers "Teeth, Artificial, Backing And Facing", a Class I medical device regulated under 21 CFR 872.3910. 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
ELK
Device Class
Class I
Regulation Number
872.3910
Submission Type
Review Panel
DE
Medical Specialty
Dental
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K811665j. adererSR-ISOCETTEJuly 15, 1981
K760909plastics/packagingTHERMOMETER JARS AND CAPSDecember 30, 1976