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