510(k) K883489

Device
KRATZ NOVA SERT(TM)
Applicant
COOPERVISION-CILCO
510(k) number
K883489
Product code
KYB  
Decision
Substantially Equivalent (SESE)
Decision date
1988-10-25
Date received
1988-08-16
Regulation
886.4300
Classification name
Lens, Guide, Intraocular
Medical specialty
Ophthalmic
Review panel
Ophthalmic
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
RAY NEGLAY
Address
3190 160th Ave. S. E. Bellevue WA US 98008 98008

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code KYB  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K152357MicroSTAAR Injector System CartridgesSTAAR Surgical Company2015-10-30
K081382DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786Duckworth & Kent, Ltd.2008-10-23
K072985DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2Duckworth & Kent, Ltd.2008-06-20
K070669IOL INJECTOR SETMedicel AG2007-11-01
K063155MONARCH III IOL DELIVERY SYSTEMAlcon Manufacturing, Ltd.2007-03-27
K063694AKREOS SINGLE USE INSERTION DEVICE, MODEL AI-28Bausch & Lomb, Inc.2007-03-07
K032412RE-USEABLE MICROSTAAR INJECTOR, MSI-SStaar Surgical Co.2004-06-10
K022723MASTEL 1 FOLDER IMPLANTATION SYSTEMMastel Precision, Inc.2002-12-26
K001157MONARCH II IOL DELIVERY SYSTEMAlcon Research, Ltd.2000-06-27
K983129DISPOSABLE MICROSTAAR INJECTOR (MODEL MSI-P1)Staar Surgical Co.1998-12-04
K981571MONARCH IOL DELIVERY SYSTEMAlcon Laboratories1998-07-09
K970033MONARCH IOL DELIVERY SYSTEMAlcon Laboratories1997-04-23
K965185ACRYPAK FOLDERAlcon Laboratories1997-03-31
K961242AMO PHACOFLEX II INTERSECTION SYSTEMAllergan, Inc.1996-06-17
K954600MICROSTAAR INJECTOR MODELS MSI-TD & MSI-PD (MODIFICATION)Staar Surgical Co.1995-12-21

Legacy Summary#

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FDA Review#

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