ClearanceBrief
Company ยท US

Ibl GmbH

FDA 510(k) clearances and medical device recalls filed under this name, 2003 to 2005. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
CHPRadioimmunoassay, Estradiol1
CHQChromatographic/Fluorometric Method, Catecholamines1
CZWComplement C3, Antigen, Antiserum, Control1
DAKComplement C1q, Antigen, Antiserum, Control1
JITCalibrator, Secondary1
JLSRadioimmunoassay, Progesterone1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 3, 2005K051969TRICAT RIA (ADRENALIN/NORADRENALIN/DOPAMINE); KATCOMBI RIA (ADRENALIN/NORADRENALIN); NORADRENALIN RIA
Ibl GmbH
CHQ
Sep 24, 2004K041349LUMINESCENT IMMUNOASSAY KIT FOR THE DETECTION OF ESTRADIOL IN SALIVA AND SERUM
Ibl GmbH
CHP
Jul 22, 2004K040923LUMINESCENT IMMUNOASSAY KIT FOR THE DETECTION OF PROGESTERONE IN SALIVA
Ibl GmbH
JLS
Feb 27, 2004K033786LUMINESCENT IMMUNOASSAY KIT FOR THE DETECTION OF TESTOSTERONE IN SERUM AND SALIVA
Ibl GmbH
JIT
Jan 13, 2004K032796IBL C3D-CIC EIA TEST
Ibl GmbH
CZW
Aug 29, 2003K032254IBL C1Q-CIC CIA TEST
Ibl GmbH
DAK

Latest recalls

DateFirm and productCodeLinked 510(k)
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