FDA 510(k) Application Details - K231288

Device Classification Name	Oximeter   More FDA Info for this Device
510(K) Number	K231288
Device Name	Oximeter
Applicant	Vyvo Technology Corp.(VT) 123 NW 23 RD Street Miami, FL 33127-4409 US Other 510(k) Applications for this Company
Contact	Alfonso Cioffi Other 510(k) Applications for this Contact
Regulation Number	870.2700   More FDA Info for this Regulation Number
Classification Product Code	DQA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/04/2023
Decision Date	03/04/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review