FDA 510(k) Application Details - K232451

Device Classification Name	Calculator, Drug Dose   More FDA Info for this Device
510(K) Number	K232451
Device Name	Calculator, Drug Dose
Applicant	Voluntis SA. 22 quai Gallieni Suresnes 92150 FR Other 510(k) Applications for this Company
Contact	Kevin Howard Other 510(k) Applications for this Contact
Regulation Number	868.1890   More FDA Info for this Regulation Number
Classification Product Code	NDC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/14/2023
Decision Date	12/12/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review