ClearanceBrief
Company ยท US

Inbios Intl., Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1999 to 2011. 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
CGAGlucose Oxidase, Glucose1
DHASystem, Test, Human Chorionic Gonadotropin1
JHIVisual, Pregnancy Hcg, Prescription Use1
LOOReagent, Leishmanii Serological1
NOPElisa, Antibody, West Nile Virus1
OSUDengue Serological Reagents1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 8, 2011DEN100020DENV DETECT IGM CAPTURE ELISA
Inbios Intl., Inc.
OSU
Nov 19, 2004K041817WEST NILE DETECT IGM ELISA
Inbios Intl., Inc.
NOP
May 6, 2003K023483KALAZAR DETECT
Inbios Intl., Inc.
LOO
Jul 26, 2000K001092GENERIC BLOOD GLUCOSE TEST STRIP
Inbios Intl., Inc.
CGA
Oct 18, 1999K992695INSURE PRO TEST
Inbios Intl., Inc.
JHI
May 28, 1999K991515INSURE PREGNANCY TEST
Inbios Intl., Inc.
DHA

Latest recalls

DateFirm and productCodeLinked 510(k)
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