Medical Device Manufacturer · US , Everett , WA

Neogenex - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 1994

Total

Cleared

Denied

Neogenex has 20 FDA 510(k) cleared medical devices. Based in Everett, US.

Historical record: 20 cleared submissions from 1994 to 1997. Primary specialty: Pathology.

Browse the FDA 510(k) cleared devices submitted by Neogenex Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Neogenex

20 devices

1-20 of 20

Cleared Feb 04, 1997

MINK LUNG CELL CULTURE

PRIMARY MONKEY KIDNEY CELL CULTURE

K943884 · KIR

Pathology · 111d

Cleared Nov 28, 1994

PRIMARY RABBIT KIDNEY CELL CULTURE

HUMAN NEWBORN FORESKIN CELL CULTURE

CHLAMYDIA TRACHOMATIS ANTIGEN TEST

K941714 · LJP

Microbiology · 117d

Cleared Jul 06, 1994

INFLUENZA A ANTIGEN TEST

K942172 · GNW

Microbiology · 62d

Cleared Jun 30, 1994

CMV EARLY ANTIGEN TEST

INFLUENZA B ANITGEN TEST

Neogenex - FDA 510(k) Cleared Devices

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