510(k) K840204

Device
WHITE OCULAR PRESSURE RELIEF DEVICE
Applicant
PRECISION-COSMET CO., INC.
510(k) number
K840204
Product code
KYF  
Decision
Substantially Equivalent (SESE)
Decision date
1985-02-15
Date received
1984-01-19
Regulation
886.3920
Classification name
Implant, Eye Valve
Medical specialty
Ophthalmic
Review panel
Ophthalmic
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
ROBERT L ULLEN
Address
11140 Bren Rd., W. Minnetonka MN US 55343 55343

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code KYF  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K230975Ahmed® Glaucoma Valve Model FP7New World Medical, Inc.2023-05-12
K231051Ahmed® Glaucoma Valve Model FP8New World Medical, Inc.2023-05-12
K220032iStent infinite Trabecular Micro-Bypass System, Model iS3Glaukos Corporation2022-08-02
K182518AHMED ClearPath Glaucoma Drainage DeviceNew World Medical, Inc.2019-01-18
K171451Ahmed Glaucoma Valve Model FP8New World Medical, Inc.2017-08-08
K161457XEN Glaucoma Treatment SystemAllergan, Inc.2016-11-21
K162060Ahmed Glaucoma ValveNew World Medical, Inc.2016-10-24
K152996Molteno3 Glaucoma ImplantInnovative Ophthalmic Products, Inc. (Iop)2015-12-17
K062252MOLTENO3Iop, Inc.2006-09-27
K060644AHMED GLAUCOMA VALVE, MODEL M4New World Medical, Inc.2006-09-18
K030350EXPRESS MINI GLAUCOMA SHUNTOptonol, Ltd.2003-03-13
K012852EX-PRESS MINATURE GLAUCOMA IMPLANT, MODELS R-20, R-30, R-50, STS VERSIONSOptonol, Ltd.2002-03-26
K991072AHMED GLAUCOMA VALVE IMPLANTNew World Medical, Inc.1999-07-13
K980657AHMED GLAUCOMA VALVE, MODEL S3New World Medical, Inc.1998-04-20
K955455BAERVELT PARS PLANA GLAUCOMA IMPLANTPharmacia Iovision, Inc.1997-02-18

Legacy Summary#

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FDA Review#

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