FDA 510(k) Application Details - K232028

Device Classification Name	Gastroscope And Accessories, Flexible/Rigid   More FDA Info for this Device
510(K) Number	K232028
Device Name	Gastroscope And Accessories, Flexible/Rigid
Applicant	IQ Endoscopes Limited Basepoint Business Centre, Riverside Court Beaufort Park Way Chepstow NP16 5UH GB Other 510(k) Applications for this Company
Contact	Chris Jenkins Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	FDS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/07/2023
Decision Date	11/17/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review