510(k) K010617

Device
SPIFE IFE CALIBRATOR AND CONTROL KIT
Applicant
Helena Laboratories
510(k) number
K010617
Product code
DEW
Decision
Substantially Equivalent (SESE)
Decision date
2001-03-15
Date received
2001-03-01
Regulation
866.5510
Classification name
Igg, Antigen, Antiserum, Control
Medical specialty
Immunology
Review panel
Immunology
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
N

Applicant Contact#

Contact
PAT FRANKS
Address
1530 Lindbergh Dr. P.O. Box 752 Beaumont TX US 77704 77704

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
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K943997BEHRING NEPHELOMETER IIBehring Diagnostics, Inc.1994-10-03
K934324OT IGG SORBENTOrganon Teknika Corp.1994-04-21
K933314RADIAS FERRITIN ENZYME IMMUNOASSAYBio-Rad1993-09-08
K924197ZORBA(TM) IGG REMOVAL REAGENTZeus Scientific, Inc.1992-12-15