510(k) K013213

Device
HYPERION VISIQUANT ANA TEST KIT
Applicant
HYPERION, INC.
510(k) number
K013213
Product code
DHN  
Decision
Substantially Equivalent (SESE)
Decision date
2002-06-04
Date received
2001-09-26
Regulation
866.5100
Classification name
Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control
Medical specialty
Immunology
Review panel
Immunology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
RADHA GOOLABSINGH
Address
14100 SW 136th St. Miami FL US 33186 33186

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code DHN  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K201956Zeus IFA ANA HEp-2 Test System, Zeus dIFineZeus Scientific, Inc.2022-04-29
K172745ImmuGlo HEp-2 Elite IFAImmco Diagnostics, Inc.2018-06-05
K153117AESKUSLIDES ANA HEp-2-Gamma, HELIOS FULLY AUTOMATED IFA SYSTEMAesku Systems GmbH&Co.Kg2016-07-28
K160265Image Navigator by Immuno ConceptsImmuno Concepts, N.A. , Ltd.2016-06-17
K141827EUROIMMUN IFA 40: HEP-20-10; EUROPATTERN MICROSCOPE AND SOFTWAREEuroimmun Us, Inc.2015-04-17
K150155NOVA Lite DAPI ANA KitInova Diagnostics, Inc.2015-04-08
K131791IFA 40: HEP-20-10Euroimmun US2014-02-26
K120889AESKUSLIDES ANA HEP-2Aesku Diagnostics2012-10-15
K070763EUROIMMUN ANA IFA: HEP-20-10Euroimmun Us, LLC2007-05-22
K042680RHIGENE HEP-ANA TEST SYSTEMCorgenix, Inc.2004-11-19
K024220LIQUICHEK AUTOIMMUNE NEGATIVE CONTROL, CATALOG #130Bio-Rad2003-01-17
K024217LIQUICHEK ANA CONTROL, SPECKLED PATTERN, POSITIVE, CATALOG #108Bio-Rad2003-01-15
K024221LIQUICHEK ANA CONTROL HOMOGENEOUS PATTERN CONTROL, POSOTIVE, CATALOG #118Bio-Rad2003-01-15
K024222LIQUICHEK ANA CONTROL CENTROMERE PATTERN, POSITIVE, CATALOG #112Bio-Rad2003-01-15
K024224LIQUICHEK ANTI-SMOOTH MUSCLE CONTROL, POSITIVE, CATALOG #129Bio-Rad2003-01-15

Legacy Summary#

summary

FDA Review#

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