510(k) K914051

PEDIATRIC VITRECTOMY LENS SET by Ocular Instruments, Inc. — Product Code HJK

K914051 is an FDA 510(k) premarket notification submitted by Ocular Instruments, Inc. for the device "PEDIATRIC VITRECTOMY LENS SET". The FDA issued a decision of Substantially Equivalent on December 9, 1991. 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
December 9, 1991
Date Received
September 10, 1991
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