Medical Device Manufacturer · US , Everett , WA

Neogenex - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 1994

20

Total

20

Cleared

0

Denied

FDA 510(k) Regulatory Record - Neogenex Pathology ✕

13 devices

1-13 of 13

Cleared Nov 28, 1994

PRIMARY MONKEY KIDNEY CELL CULTURE

Pathology · 111d

Cleared Nov 28, 1994

PRIMARY RABBIT KIDNEY CELL CULTURE

Pathology · 111d

Cleared Nov 28, 1994

BGM CELL CULTURE

Pathology · 111d

Cleared Nov 28, 1994

HUMAN NEWBORN FORESKIN CELL CULTURE

Pathology · 111d

Cleared Nov 28, 1994

MDCK CELL CULTURE

Pathology · 111d

Cleared Nov 28, 1994

VERO CELL CULTURE

Pathology · 111d

Cleared Nov 28, 1994

WI38 CELL CULTURE

Pathology · 111d

Cleared Nov 28, 1994

RD CULTURE CELL

Pathology · 111d

Cleared Mar 31, 1994

HEP-2 CULTURE CELL

Pathology · 233d

Cleared Mar 29, 1994

A549 CULTURE CELL

Pathology · 231d

Cleared Mar 29, 1994

MCCOY CULTURE CELL

Pathology · 231d

Cleared Mar 29, 1994

MRC-5 CULTURE CELL

Pathology · 231d

Cleared Mar 29, 1994

LLCMK2 CULTURE CELLS

Pathology · 231d