Product code MMQ— Ophthalmic

FDA has cleared 5 devices under product code MMQ between 1995 and 1998, 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.

• 19981 clearance
• 19972 clearances
• 19961 clearance
• 19951 clearance

• Par Vision Systems Corp.1 clearance
• Orbtek, Inc.1 clearance
• Euclid Systems Corp.1 clearance
• Eclipse Ventures1 clearance
• Bio-Medical Sciences, Inc.1 clearance

• K981665 — SILON TOPOMAT CORNEAL TOPOGRAPHY IMAGE ENHANCEMENT DEVICEBio-Medical Sciences, Inc.·1998-12-07
• K964702 — EUCLID SYSTEMS CORNEAL TOPOGRAPHER MODEL ET800Euclid Systems Corp.·1997-05-20
• K964891 — ORBSHOT KERATOMETEROrbtek, Inc.·1997-03-26
• K963762 — CORNEAL TOPOGRAPHER 200Eclipse Ventures·1996-12-23
• K950077 — INTRAOPERATIVE CORNEAL TOPOGRAPHY SYSTEM (I-CTS)Par Vision Systems Corp.·1995-06-14