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510(k) K924774

Device
BURTON AUTOMATIC PROJECTOR - MODEL CP-40
Applicant
R.H. BURTON CO.
510(k) number
K924774
Product code
HOD  
Decision
Substantially Equivalent (SESE)
Decision date
1993-04-14
Date received
1992-09-23
Regulation
886.4350
Classification name
Clamp, Eyelid, Ophthalmic
Medical specialty
Ophthalmic
Review panel
Ophthalmic
Device class
1
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
KEVIN M LOYCHIK
Address
3965 Brookham Dr. P.O. Box 68 Grove City OH US 43123 43123

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code HOD  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K891610HENSON CFA 3000 CENTRAL VISUAL FIELD SCREENERKeeler Instruments, Inc.1989-06-05
K831285SURGICAL/LID MARGIN COVER & EYELASH-Richard R. Anthony, M.D.1983-06-03

Legacy Summary#

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FDA Review#

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