510(k) K871099

SCHIRMER NYLON SUTURE LASER LENS by Ocular Instruments, Inc. — Product Code LQJ

K871099 is an FDA 510(k) premarket notification submitted by Ocular Instruments, Inc. for the device "SCHIRMER NYLON SUTURE LASER LENS". The FDA issued a decision of Substantially Equivalent on April 27, 1987. The device falls under product code LQJ (Lens, Surgical, Laser, Accesssory, Ophthalmic Laser), a Class II device regulated under 21 CFR 886.4390. Ocular Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 27, 1987
Date Received
March 19, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Lens, Surgical, Laser, Accesssory, Ophthalmic Laser
Device Class
Class II
Regulation Number
886.4390
Review Panel
OP
Submission Type