Cleared Traditional

LANDERS VITRECTOMY LENS RING W/INFUSION

K902496 · Ocular Instruments, Inc. · Ophthalmic
Jul 1990
Decision
49d
Days
Class 1
Risk

About This 510(k) Submission

K902496 is an FDA 510(k) clearance for the LANDERS VITRECTOMY LENS RING W/INFUSION, a Ring, Ophthalmic (flieringa) (Class I — General Controls, product code HNH), submitted by Ocular Instruments, Inc. (Bellevue, US). The FDA issued a Cleared decision on July 24, 1990, 49 days after receiving the submission on June 5, 1990. This device falls under the Ophthalmic review panel. Regulated under 21 CFR 886.4350.

Submission Details

510(k) Number K902496 FDA.gov
FDA Decision Cleared SESE
Date Received June 05, 1990
Decision Date July 24, 1990
Days to Decision 49 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary —

Device Classification

Product Code HNH — Ring, Ophthalmic (flieringa)
Device Class Class I — General Controls
CFR Regulation 21 CFR 886.4350

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