FDA 510(k) Application Details - K190167

Device Classification Name	Catheter, Steerable   More FDA Info for this Device
510(K) Number	K190167
Device Name	Catheter, Steerable
Applicant	Abbott 3200 Lakeside Drive Santa Clara, CA 95054 US Other 510(k) Applications for this Company
Contact	Ekta Lad Other 510(k) Applications for this Contact
Regulation Number	870.1280   More FDA Info for this Regulation Number
Classification Product Code	DRA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/31/2019
Decision Date	05/29/2019
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review