Product code HOJ— Ophthalmic

FDA has cleared 3 devices under product code HOJ between 1982 and 1987, filed by 3 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.

• 19871 clearance
• 19841 clearance
• 19821 clearance

• Richmond Products, Inc.1 clearance
• Pro Design Intl. AS1 clearance
• Medical Equipment Designs, Inc.1 clearance

• K873919 — TANGENT SCREENRichmond Products, Inc.·1987-10-28
• K844657 — SPECTABLE FRAME MAGNIFYING BRILLETTEPro Design Intl. AS·1984-12-11
• K821081 — CHART PROJECTORMedical Equipment Designs, Inc.·1982-06-14