510(k) K933264

RITCH NYLON SUTURE LASER LENS by Ocular Instruments, Inc. — Product Code HJK

K933264 is an FDA 510(k) premarket notification submitted by Ocular Instruments, Inc. for the device "RITCH NYLON SUTURE LASER LENS". The FDA issued a decision of Substantially Equivalent on October 31, 1994. The device falls under product code HJK (Lens, Contact, Polymethylmethacrylate, Diagnostic), a Class II device regulated under 21 CFR 886.1385. Ocular Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 31, 1994
Date Received
July 6, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Lens, Contact, Polymethylmethacrylate, Diagnostic
Device Class
Class II
Regulation Number
886.1385
Review Panel
OP
Submission Type