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510(k) K820526

Device
RELIEF VALVE-HONAN INTRAOC. PRESSURE
Applicant
THE LEBANON CORP.
510(k) number
K820526
Product code
LCC  
Decision
Substantially Equivalent (SESE)
Decision date
1982-03-25
Date received
1982-02-26
Regulation
886.4610
Classification name
Applicator, Ocular Pressure
Medical specialty
Ophthalmic
Review panel
Ophthalmic
Device class
2
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 LCC  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K112952ILWAIT TIMER OCULOPRESSOROryx Medical Pty, Ltd.2012-05-10
K946194WEE BAG O'MERCURYMicrosurgical Technology, Inc.1995-02-27
K852032OCULAR PRESSURE REDUCER (MCCANNEL)Visitec Co.1985-08-12
K840004WEE BAG O'MERCURYSurgi-Quip Inc.U1984-03-22
K792255NEVYAS AUTOPRESS EYE COMPRESSORKeeler Optical Products , Ltd.1979-12-11

Legacy Summary#

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FDA Review#

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