Medical Device Manufacturer · US , Mountain View , CA

Alexon, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1991

Total

Cleared

Denied

Alexon, Inc. has 10 FDA 510(k) cleared microbiology devices. Based in Mountain View, US.

Historical record: 10 cleared submissions from 1991 to 1994.

Browse the complete list of FDA 510(k) cleared microbiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Alexon, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Alexon, Inc.

10 devices

1-10 of 10

Cleared Sep 20, 1994

PROSPECT MICROPLATE ASSAY

PROSPECT(TM) GIARDIA RAPID ASSAY, MODIFICATION

K931147 · MHI

Microbiology · 69d

Cleared Apr 21, 1993

PROSPEC T GIARDIA MICROTITER ASSAY

K930451 · MHI

Microbiology · 84d

Cleared Sep 11, 1992

PROSPECT GIARDIA CONTROLS

K922675 · MHI

Microbiology · 99d

Cleared Jun 19, 1992

PROSPECT(TM) GIARDIA MICROTITER ASSAY/MODIFICATION

K922010 · MHI

Microbiology · 50d

Cleared Apr 22, 1992

MODIFICATION PROSPECT GIARDIA RAPID ASSAY

K920817 · MHI

Microbiology · 76d

Cleared Mar 23, 1992

PROSPECT(TM/CRYPTOSPORIDIUM

K912242 · MHJ

Microbiology · 307d

Cleared Jan 30, 1992

PROSPECT(TM) GIARDIA RAPID ASSAY

K915093 · MHI

Microbiology · 79d

Cleared Sep 27, 1991

PROSPEC T/GIARDIA RAPID ASSAY

K911337 · MHI

Microbiology · 185d

Alexon, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Alexon, Inc.

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