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FDA Product Code

FDA Product Code HOI — Clearance Directory

Device Class
Class I
Assigned Panel
Ophthalmic
21 CFR Citation
886.5840

510(k) Clearances — 11 records

K-Number Device Name Applicant Decision Date Clearance Type Summary
K943613 NIL Sing Wah International Enterprises , Ltd. 1994-09-21 Traditional PDF ↗
K930435 SPECTACLE FRAMES Venis DI A. Vendrame 1993-09-20 Traditional PDF ↗
K931328 PYRAMID SUNGLASSES/PYRAMID READING GLASSES Pyramid 1993-08-10 Traditional PDF ↗
K910329 SUNGLASSES Cutler & Gross Sloan Optical , Ltd. 1991-03-12 Traditional PDF ↗
K854854 SYSTEMS OF SIGHT LOW VISION EYEWARE Int'L Eye Care, Inc. 1986-02-04 Traditional PDF ↗
K844716 MAGNIFYING SPECTACLES W/PLASTIC LENSES Gazelle Corp. 1985-01-03 Traditional PDF ↗
K844038 VISITEC MAGNIFYING SPECTACLES Visitec Co. 1984-11-29 Traditional PDF ↗
K842835 BRILLETTE MODEL Cillus Company, Inc. 1984-11-21 Traditional PDF ↗
K820732 LA VEL LATERAL VIEW EXTENSION LENS Peter M. Tolliver 1982-05-03 Traditional PDF ↗
K813548 UVEX MINI-SPECS Bacou USA, Inc. and Uvex Safety, Inc. 1982-03-02 Traditional PDF ↗
K801733 FENZL RETICLE Robert E. Fenzl, M.D. 1980-09-16 Traditional PDF ↗

Product code HOI · Class I · Ophthalmic. Data: openFDA.