ClearanceBrief
Company ยท US

Kabivitrum, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 1988. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GGPTest, Qualitative And Quantitative Factor Deficiency3
DDXPlasminogen, Antigen, Antiserum, Control1
JBQAntithrombin Iii Quantitation1
KFFAssay, Heparin1
KPEContainer, I.V.1
LGPAssay, Alpha-2-Antiplasmin1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 13, 1988K884058COATEST PROTEIN C
Kabivitrum, Inc.
GGP
Feb 26, 1986K854572COATEST PLASMINOGEN
Kabivitrum, Inc.
DDX
May 6, 1985K844664THE I.V. BAG
Kabivitrum, Inc.
KPE
Jan 30, 1984K833892COATEST FACTOR VIII
Kabivitrum, Inc.
GGP
Jan 30, 1984K833891COATEST HEPARIN
Kabivitrum, Inc.
KFF
Jan 30, 1984K833890COATEST ANTIPLASMIN
Kabivitrum, Inc.
LGP
Aug 26, 1983K832114COATEST FACTOR X
Kabivitrum, Inc.
GGP
Dec 30, 1981K812829COATEST ANTITHROMBIN
Kabivitrum, Inc.
JBQ

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes