Medical Device Manufacturer · US , Everett , WA

Neogenex - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 1994

Recent clearances: MINK LUNG CELL CULTURE, H292 CELL CULTURE, PRIMARY MONKEY KIDNEY CELL CULTURE

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.

Neogenex is one of 15029 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Neogenex

20 devices

1-12 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

Neogenex - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Neogenex

Filters