FDA 510(k) Application Details - K233397

Device Classification Name	Catheter, Electrode Recording, Or Probe, Electrode Recording   More FDA Info for this Device
510(K) Number	K233397
Device Name	Catheter, Electrode Recording, Or Probe, Electrode Recording
Applicant	Medtronic, Inc. 8200 Coreal Sea Street NE MVS3 Mounds View, MN 55112 US Other 510(k) Applications for this Company
Contact	Karine Lortie Other 510(k) Applications for this Contact
Regulation Number	870.1220   More FDA Info for this Regulation Number
Classification Product Code	DRF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/03/2023
Decision Date	12/02/2023
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