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FDA 510(k) Applications Submitted by Bryan Kiehl
FDA 510(k) Number
Submission Date
Device Name
Applicant
K010301
02/01/2001
IMMUNOWELL EA (D) IGG TEST
GenBio
K963054
08/06/1996
IMMUNOWELL MYCOPLASMA PNEUMONIA ANTIBODY (IGM) TEST (3130)
GenBio
K963055
08/06/1996
IMMUNOWELL MYCOPLASMA PNEUMONIA ANTIBODY (IGG) TEST 3120
GenBio
K953682
08/07/1995
IMMUNO DOT BORRELIA DOT BLOT G TEST
GenBio
K953683
08/07/1995
MMUNO DOT BORRELIA DOT BLOT M TEST
GenBio
K973939
10/15/1997
IMMUNOWELL VCA IGM TEST
GenBio
K973940
10/15/1997
IMMUNOWELL EBV VCA IGG TEST
GenBio
K973941
10/15/1997
IMMUNOWELL EBNA IGG TEST
GenBio
K974226
11/12/1997
IMMUNODOT MONO-G TEST
GenBio
K974244
11/12/1997
IMMUNODOT MONO-M TEST
GenBio
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