Product code EHJ— Dental

FDA has cleared 4 devices under product code EHJ between 1977 and 1991, filed by 4 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

• 19911 clearance
• 19871 clearance
• 19791 clearance
• 19771 clearance

• Vermont Diamond Instruments1 clearance
• E.C. Moore Co.1 clearance
• Centrix, Inc.1 clearance
• Cavitron Corp.1 clearance

• K911111 — MICROMILLS, PATRIOTS, ALPHA GOLD DIAMONDSVermont Diamond Instruments·1991-11-19
• K873002 — MIN-IDENTOFLEXCentrix, Inc.·1987-08-17
• K790640 — HOWMEDICA BRASS CENTER DISCE.C. Moore Co.·1979-05-01
• K771658 — IDENTOFLEXCavitron Corp.·1977-09-12