FDA 510(k) Application Details - K232902

Device Classification Name	Insufflator, Laparoscopic   More FDA Info for this Device
510(K) Number	K232902
Device Name	Insufflator, Laparoscopic
Applicant	Palliare Ltd. Galway Business Park, Dangan Galway H91 P2DK IE Other 510(k) Applications for this Company
Contact	John O'Dea Other 510(k) Applications for this Contact
Regulation Number	884.1730   More FDA Info for this Regulation Number
Classification Product Code	HIF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/18/2023
Decision Date	05/02/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review