FDA 510(k) Application Details - K173817

Device Classification Name	Manual Antimicrobial Susceptibility Test Systems   More FDA Info for this Device
510(K) Number	K173817
Device Name	Manual Antimicrobial Susceptibility Test Systems
Applicant	Liofilchem s. r. l. Via Scozia zona ind.le Roseto degli Abruzzi 64026 IT Other 510(k) Applications for this Company
Contact	Fabio Brocco Other 510(k) Applications for this Contact
Regulation Number	866.1640   More FDA Info for this Regulation Number
Classification Product Code	JWY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/15/2017
Decision Date	02/28/2018
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