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EKI — Carrier, Amalgam, Operative Class I

FDA Device Classification

Classification Details

Product Code
EKI
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
K945220buffalo dental mfg. coAMALGAM CARRIERJanuary 11, 1995
K781034premier dental productsPREMIER INLAY PLACERJune 30, 1978