FDA 510(k) Application Details - K210924

Device Classification Name	Thermometer, Electronic, Clinical   More FDA Info for this Device
510(K) Number	K210924
Device Name	Thermometer, Electronic, Clinical
Applicant	BodyCAP 3 Dr. Laennec Street Herouville Saint Clair 14200 FR Other 510(k) Applications for this Company
Contact	SΘbastien Moussay Other 510(k) Applications for this Contact
Regulation Number	880.2910   More FDA Info for this Regulation Number
Classification Product Code	FLL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/29/2021
Decision Date	06/28/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review