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FDA 510(k) Applications Submitted by WIESLAB AB
FDA 510(k) Number
Submission Date
Device Name
Applicant
K974166
11/05/1997
WIELISA MPO ANCA TEST SYSTEM
WIESLAB AB
K974167
11/05/1997
WIELISA PR-3 ANCA TEST SYSTEM
WIESLAB AB
K974169
11/05/1997
WIELISA ANTI-GBM TEST SYSTEM
WIESLAB AB
K981750
05/18/1998
WIELISA ANTI-GBM, ANCA SCREENING KIT TEST SYSTEM
WIESLAB AB
K981748
05/18/1998
WIELISA ANCA SCREENING KIT TEST SYSTEM
WIESLAB AB
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