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510(k) K801733

Device
FENZL RETICLE
Applicant
ROBERT E. FENZL, M.D.
510(k) number
K801733
Product code
HOI  
Decision
Substantially Equivalent (SESE)
Decision date
1980-09-16
Date received
1980-07-25
Regulation
886.5840
Classification name
Spectacle, Magnifying
Medical specialty
Ophthalmic
Review panel
Ophthalmic
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code HOI  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K943613NILSing Wah International Enterprises , Ltd.1994-09-21
K930435SPECTACLE FRAMESVenis DI A. Vendrame1993-09-20
K931328PYRAMID SUNGLASSES/PYRAMID READING GLASSESPyramid1993-08-10
K910329SUNGLASSESCutler & Gross Sloan Optical , Ltd.1991-03-12
K854854SYSTEMS OF SIGHT LOW VISION EYEWAREInt'L Eye Care, Inc.1986-02-04
K844716MAGNIFYING SPECTACLES W/PLASTIC LENSESGazelle Corp.1985-01-03
K844038VISITEC MAGNIFYING SPECTACLESVisitec Co.1984-11-29
K842835BRILLETTE MODELCillus Company, Inc.1984-11-21
K820732LA VEL LATERAL VIEW EXTENSION LENSPeter M. Tolliver1982-05-03
K813548UVEX MINI-SPECSBacou USA, Inc. and Uvex Safety, Inc.1982-03-02

Legacy Summary#

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FDA Review#

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