Medical Device Manufacturer · US , Mchenry , IL

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

129 submissions · 126 cleared · Since 1976

129

Total

126

Cleared

Denied

Pharmacia, Inc. has 126 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 126 cleared submissions from 1976 to 1998. Primary specialty: Immunology.

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

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

129 devices

1-12 of 129

1 2 3 4

Cleared Feb 09, 1998

ALLERGAN IMMUNO CAP M4, M8, K70

UNICAP SPECIFIC IGE FEIA ASSAY, LATEX ALLERGEN IMMUNOCAP K82

K972068 · DHB

Immunology · 30d

Cleared Jun 30, 1997

MASTERCAP AM 5.0/MASTERCAP RM 5.0

K970420 · JQW

Chemistry · 147d

Cleared Apr 23, 1997

UNICAP TOTAL IGE ASSAY/PHARMACIA TOTAL IGE CONTROLS LMH

PHARMACIA CAP SYSTEM PHADIATOP FEIA

General Hospital · 56d

Cleared Oct 19, 1995

PISTON SYRINGE

K951025 · FMF

General Hospital · 227d

ALLERGANS PHARMACIA CAP SYS.RAST RIA/FEIA

K911903 · DHB

Immunology · 105d

Cleared Apr 24, 1991

PHARMACIA SPECIFIC IGE CONTROL

K911631 · DGC

Immunology · 13d

1 2 3 4

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

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