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510(k) K800666

Device
QUIK-TEMP
Applicant
LIQUID CRYSTAL PRODUCTS, INC.
510(k) number
K800666
Product code
KPP  
Decision
Substantially Equivalent (SESE)
Decision date
1980-05-08
Date received
1980-03-26
Regulation
876.5630
Classification name
Peritoneal Dialysate Filter
Medical specialty
Gastroenterology/Urology
Review panel
Gastroenterology/Urology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code KPP  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K812615TM-CAPDTri-Med, Inc.1982-01-05
K803275KPP PERITONEAL DIALYSATE FILTERMillipore Corp.1981-03-13

Legacy Summary#

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FDA Review#

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