Product code JYJ— Ear, Nose, Throat

FDA has cleared 5 devices under product code JYJ between 1980 and 1991, filed by 4 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
• 19891 clearance
• 19881 clearance
• 19841 clearance
• 19801 clearance

• Suredrop, Inc.2 clearances
• Microtek Medical, Inc.1 clearance
• Kc Medical Industries1 clearance
• Aztec Medical Products, Inc.1 clearance

• K904469 — EYEOPENERKc Medical Industries·1991-06-28
• K884974 — ACCESSORY TO EYEDROP GUIDESuredrop, Inc.·1989-03-24
• K874569 — SUREDROP EYEDROP GUIDESuredrop, Inc.·1988-05-03
• K833606 — IMPLANT MEASURING GAUGEMicrotek Medical, Inc.·1984-01-03
• K801938 — RHINOMETERAztec Medical Products, Inc.·1980-09-09