IGG FLEX REAGENT CARTRIDGE

Radioimmunoassay, Immunoglobulins (g, A, M)

DADE BEHRING, INC.

The following data is part of a premarket notification filed by Dade Behring, Inc. with the FDA for Igg Flex Reagent Cartridge.

Pre-market Notification Details

Device IDK990551
510k NumberK990551
Device Name:IGG FLEX REAGENT CARTRIDGE
ClassificationRadioimmunoassay, Immunoglobulins (g, A, M)
Applicant DADE BEHRING, INC. P.O. BOX 6101 ROUTE 896, GLASGOW BLDG. 500 Newark,  DE  19714 -6101
ContactCathy P Craft
CorrespondentCathy P Craft
DADE BEHRING, INC. P.O. BOX 6101 ROUTE 896, GLASGOW BLDG. 500 Newark,  DE  19714 -6101
Product CodeCFQ  
CFR Regulation Number866.5510 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1999-02-22
Decision Date1999-03-25
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00842768005701 K990551 000

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