Product code LQJ— Ophthalmic

FDA has cleared 13 devices under product code LQJ between 1986 and 2017, filed by 7 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

• 20171 clearance
• 19931 clearance
• 19921 clearance
• 19911 clearance
• 19891 clearance
• 19884 clearances
• 19873 clearances
• 19861 clearance

• Ocular Instruments, Inc.6 clearances
• California Laboratories, Inc.2 clearances
• Tomey Corporation USA1 clearance
• Sorenson Laboratories, Inc.1 clearance
• Katalyst Surgical, LLC1 clearance
• Chiron Vision Corp.1 clearance
• Biophysic Medical, Inc.1 clearance

• K163632 — Katalyst Cyclophotocoagulation ProbeKatalyst Surgical, LLC·2017-06-15
• K931356 — SAFE AIR VARI-SPOT HANDPIECE TELESCOPE AND ADAPTORSorenson Laboratories, Inc.·1993-09-07
• K921414 — TROKEL /3 GONIO LASER LENSOcular Instruments, Inc.·1992-11-16
• K912112 — PF-400,GF-300,IF-200,PG400,PG400C,AND ED-480Tomey Corporation USA·1991-06-17
• K893731 — SHIELDS T.C. LASER LENSOcular Instruments, Inc.·1989-08-17
• K884694 — MQL 20 ND:YAG OPHTHALMIC LASERCalifornia Laboratories, Inc.·1988-11-30
• K883719 — INTERCONN. OF OPHTHALAS & NANOLAS LASER SYSTEMBiophysic Medical, Inc.·1988-10-18
• K883270 — IRIS ND:YAG OPTHALMIC LASERCalifornia Laboratories, Inc.·1988-10-13
• K882574 — BOLDREY PERIPHERAL RETINAL LENSOcular Instruments, Inc.·1988-07-29
• K872802 — TROKEL SINGLE MIRROR YAG LASER LENSOcular Instruments, Inc.·1987-09-04
• K871245 — LASER CONTACT LENSES CGA 1, CGI 1, CGP 1, CGV 1Chiron Vision Corp.·1987-05-07
• K871099 — SCHIRMER NYLON SUTURE LASER LENSOcular Instruments, Inc.·1987-04-27
• K862869 — PETRUS SINGLE MIRROR LASER LENSOcular Instruments, Inc.·1986-08-21