510(k) K022413

Device
LUNEAU 3 MIRROR LENS
Applicant
Luneau SA
510(k) number
K022413
Product code
HJK
Decision
Substantially Equivalent (SESE)
Decision date
2002-09-24
Date received
2002-07-24
Regulation
886.1385
Classification name
Lens, Contact, Polymethylmethacrylate, Diagnostic
Medical specialty
Ophthalmic
Review panel
Ophthalmic
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
N

Applicant Contact#

Contact
JEAN NOEL YOUNG
Address
Bp 252 Chartres Cedex FR 28005 28005

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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510(k), Device, Applicant table
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K050623VOLK DISPOSABLE VITRECTOMY LENSES, MODELS VOLK FLAT SSV D, VOLK AFX SSV D, VOLK 45 PRISM SSV DVolk Optical, Inc.2005-03-28
K033950DORC VITRECTOMY LENSES, MODEL 1284 SERIESDutch Ophthalmic Research Center (D.O.R.C.)2004-02-20
K030054DISPOSABLE VITRECTOMY SETS, DISPOSABLE VIRECTOMY LENSESFci Ophthalmics, Inc.2003-02-26
K023221CONTACT LASER & DIAGNOSTIC LENSESVolk Optical, Inc.2002-10-11
K014170STAURENGHI WIDE FIELD SCANNING LASER LENSOcular Instruments, Inc.2002-03-04
K012096DISPOSABLE VITRECTOMY LENSOcular Instruments, Inc.2001-08-24
K971853ENDOVIEW SPPHIRE LENS SETAmerican Medical Devices, Inc.1997-08-06
K933976MANDELKORN SUTURE LYSIS LENSOcular Instruments, Inc.1994-11-08
K933264RITCH NYLON SUTURE LASER LENSOcular Instruments, Inc.1994-10-31