Product code EHB— Dental

FDA has cleared 5 devices under product code EHB between 1978 and 1992, filed by 5 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.

• 19921 clearance
• 19901 clearance
• 19842 clearances
• 19781 clearance

• S.C.D.P.I. of Florida, Inc.1 clearance
• Moyco Industries, Inc.1 clearance
• Knochen Dental Laboratory1 clearance
• Innovators, Inc.1 clearance
• General X-Ray, Inc.1 clearance

• K921355 — WINGMASTERInnovators, Inc.·1992-09-25
• K903012 — AUDIOPRAT ENDOSCOPES.C.D.P.I. of Florida, Inc.·1990-10-09
• K834606 — X-RAY COLLIMATOR X-CJDKnochen Dental Laboratory·1984-02-21
• K833558 — X-RAY SHIELDMoyco Industries, Inc.·1984-01-13
• K781675 — X-RAY COLLIMATORGeneral X-Ray, Inc.·1978-12-04