FDA 510(k) Application Details - K220016

Device Classification Name	Reagent, Borrelia Serological Reagent   More FDA Info for this Device
510(K) Number	K220016
Device Name	Reagent, Borrelia Serological Reagent
Applicant	Viramed Biotech AG Behringstrasse 11 Planegg 82152 DE Other 510(k) Applications for this Company
Contact	Martin Kintrup Other 510(k) Applications for this Contact
Regulation Number	866.3830   More FDA Info for this Regulation Number
Classification Product Code	LSR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/05/2022
Decision Date	08/19/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	MI - Microbiology
Review Advisory Committee	MI - Microbiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review