FDA 510(k) Application Details - K230812

Device Classification Name	Electrocardiograph   More FDA Info for this Device
510(K) Number	K230812
Device Name	Electrocardiograph
Applicant	Withings 2 rue Maurice Hartmann Issy-Les-Moulineaux 92130 FR Other 510(k) Applications for this Company
Contact	Khushboo Surendran Other 510(k) Applications for this Contact
Regulation Number	870.2340   More FDA Info for this Regulation Number
Classification Product Code	DPS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/24/2023
Decision Date	08/23/2023
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