510(k) K902496

LANDERS VITRECTOMY LENS RING W/INFUSION by Ocular Instruments, Inc. — Product Code HNH

K902496 is an FDA 510(k) premarket notification submitted by Ocular Instruments, Inc. for the device "LANDERS VITRECTOMY LENS RING W/INFUSION". The FDA issued a decision of Substantially Equivalent on July 24, 1990. The device falls under product code HNH (Ring, Ophthalmic (Flieringa)), a Class I device regulated under 21 CFR 886.4350. Ocular Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 24, 1990
Date Received
June 5, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ring, Ophthalmic (Flieringa)
Device Class
Class I
Regulation Number
886.4350
Review Panel
OP
Submission Type