FDA 510(k) Application Details - K182297

Device Classification Name	Transmitters And Receivers, Physiological Signal, Radiofrequency   More FDA Info for this Device
510(K) Number	K182297
Device Name	Transmitters And Receivers, Physiological Signal, Radiofrequency
Applicant	Mortara Instrument Inc 7865 North 86th Street Milwaukee, WI 53224 US Other 510(k) Applications for this Company
Contact	Marco Manduchi Other 510(k) Applications for this Contact
Regulation Number	870.2910   More FDA Info for this Regulation Number
Classification Product Code	DRG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/24/2018
Decision Date	01/24/2019
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review