FDA 510(k) Application Details - K240598

Device Classification Name	Table, Operating-Room, Ac-Powered   More FDA Info for this Device
510(K) Number	K240598
Device Name	Table, Operating-Room, Ac-Powered
Applicant	Moon Surgical 9 rue dÆEnghien Paris 75010 FR Other 510(k) Applications for this Company
Contact	Anne Osdoit Other 510(k) Applications for this Contact
Regulation Number	878.4960   More FDA Info for this Regulation Number
Classification Product Code	FQO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/04/2024
Decision Date	06/03/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review