FDA 510(k) Application Details - K233825

Device Classification Name	Catheter, Recording, Electrode, Reprocessed   More FDA Info for this Device
510(K) Number	K233825
Device Name	Catheter, Recording, Electrode, Reprocessed
Applicant	Innovative Health 1435 N. Hayden Rd Suite 100 Scottsdale, AZ 85257 US Other 510(k) Applications for this Company
Contact	Meerna Muradvich Other 510(k) Applications for this Contact
Regulation Number	870.1220   More FDA Info for this Regulation Number
Classification Product Code	NLH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/01/2023
Decision Date	06/07/2024
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