Medical Device Manufacturer · US , Frederick , MD

Wieslab AB

5 submissions · 5 cleared · Since 1998
5
Total
5
Cleared
0
Denied

Wieslab AB has 5 FDA 510(k) cleared medical devices. Based in Frederick, US.

Historical record: 5 cleared submissions from 1998 to 1998. Primary specialty: Immunology.

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

5 devices
1–5 of 5
WIELISA ANCA SCREENING KIT TEST SYSTEM
K981748 · MOB Test System, Antineutrophil Cytoplasmic Antibodies (anca) · Immunology
Jul 1998 65d
WIELISA ANTI-GBM, ANCA SCREENING KIT TEST SYSTEM
K981750 · MOB Test System, Antineutrophil Cytoplasmic Antibodies (anca) · Immunology
Jul 1998 65d
WIELISA MPO ANCA TEST SYSTEM
K974166 · MOB Test System, Antineutrophil Cytoplasmic Antibodies (anca) · Immunology
Feb 1998 104d
WIELISA PR-3 ANCA TEST SYSTEM
K974167 · MOB Test System, Antineutrophil Cytoplasmic Antibodies (anca) · Immunology
Feb 1998 104d
WIELISA ANTI-GBM TEST SYSTEM
K974169 · DBL Multiple Autoantibodies, Indirect Immunofluorescent, Antigen, Control · Immunology
Feb 1998 104d
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