Medical Device Manufacturer · US , Mchenry , IL

Viromed Laboratories, Inc. - FDA 510(k) Cleared Devices

25 submissions · 25 cleared · Since 1983

Total

Cleared

Denied

Viromed Laboratories, Inc. has 25 FDA 510(k) cleared pathology devices. Based in Mchenry, US.

Historical record: 25 cleared submissions from 1983 to 1996.

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

Viromed Laboratories, 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 - Viromed Laboratories, Inc.

25 devices

1-12 of 25

Cleared May 22, 1996

LLC-MK2 (MONKEY KIDNEY, MACACA MULATA) CELL CULTURE

K951440 · KIR

Pathology · 420d

Cleared May 22, 1996

NCI-H292 CELL CULTURE

K951461 · KIR

Pathology · 419d

Cleared May 13, 1987

BUFFALO GREEN MONKEY KIDNEY CELLS

K871613 · KIR

Pathology · 19d

Cleared Jul 10, 1986

HUMAN EPITHELOID CERVIX CARCINOMA CELLS (HELA)

K862555 · KIR

Pathology · 7d

Cleared Apr 18, 1986

HUMAN LUNG CARCINOMA CELLS (A549)

K861373 · KIR

Pathology · 7d

Cleared Dec 04, 1985

RESPIRATORY SYNCYTIAL VIRUS ID REAGENT

AFRICAN GREEN SV 5/SV 40

K843252 · KIR

Pathology · 17d

Viromed Laboratories, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Viromed Laboratories, Inc.

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