EHO — Bar, Preformed Class I

FDA Device Classification

FDA product code EHO covers "Bar, Preformed", a Class I medical device regulated under 21 CFR 872.3165. 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
EHO
Device Class
Class I
Regulation Number
872.3165
Submission Type
Review Panel
DE
Medical Specialty
Dental
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K934468gatewood splintsSLIP-ON FIXATION SPLINT (SFS)August 5, 1994
K881133trophy radiologie70-X/RVG (RADIOVISIOGRAPHY)July 20, 1989
K883388dale t. dupuisDENTREK BRIDGE BARSOctober 6, 1988