FDA 510(k) Application Details - K233056

Device Classification Name	Syringe, Piston   More FDA Info for this Device
510(K) Number	K233056
Device Name	Syringe, Piston
Applicant	GuideStar Medical Devices 201-2067 Cadboro Bay Road Victoria V8R 5G4 CA Other 510(k) Applications for this Company
Contact	Michael Dolphin Other 510(k) Applications for this Contact
Regulation Number	880.5860   More FDA Info for this Regulation Number
Classification Product Code	FMF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/25/2023
Decision Date	11/02/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	Y
Expedited Review