Product code HOQ— Ophthalmic

FDA has cleared 8 devices under product code HOQ between 1985 and 2018, filed by 6 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.

• 20181 clearance
• 20151 clearance
• 20131 clearance
• 20021 clearance
• 19881 clearance
• 19871 clearance
• 19852 clearances

• Wheel Checkers2 clearances
• Vital Art and Science Incorporated2 clearances
• Richmond Products, Inc.1 clearance
• Oculocare Medical AG1 clearance
• Notal Vision, Inc.1 clearance
• Danek Medical, Inc.1 clearance

• K180895 — AlleyeOculocare Medical AG·2018-06-27
• K143211 — myVision Track Model 005Vital Art and Science Incorporated·2015-03-20
• K121738 — MYVISIONTRACK(TM)Vital Art and Science Incorporated·2013-02-22
• K014044 — MASCULAR COMPUTERIZED PSYCHOPHYSICAL TEST (MCPT)Notal Vision, Inc.·2002-03-04
• K874252 — KREDA DISCRichmond Products, Inc.·1988-01-27
• K863429 — MODIFIED DEVICE FOR SELF EXAMINATION OF EYESWheel Checkers·1987-01-20
• K843227 — MACULAR FUNCTION ANALYZERDanek Medical, Inc.·1985-07-22
• K843702 — APPARATUS & METHODS SELF-EXAM OF EYEWheel Checkers·1985-01-03