Product code KYD— Ophthalmic

FDA has cleared 3 devices under product code KYD between 1983 and 1991, 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.

• 19911 clearance
• 19881 clearance
• 19831 clearance

• Visionex, Inc.1 clearance
• Smith & Nephew, Inc.1 clearance
• Northland Cataract & Eye Care Clinic1 clearance

• K911734 — TEARTEC RAPID LACRIMAL ASSESMENT SYSTEMNorthland Cataract & Eye Care Clinic·1991-11-07
• K881515 — TEAR VOLUME TESTSVisionex, Inc.·1988-05-23
• K832181 — SNO STRIPS STERILE TEARFLOW TEST STRIPSmith & Nephew, Inc.·1983-08-12