FDA 510(k) Application Details - K100899

Device Classification Name	Pump, Air, Non-Manual, For Endoscope   More FDA Info for this Device
510(K) Number	K100899
Device Name	Pump, Air, Non-Manual, For Endoscope
Applicant	KEYMED (MEDICAL & INDUSTRIAL EQUIPMENT), LTD. 11440 WEST BERNARDO DRIVE SUITE 300 SAN DIEGO, CA 92127 US Other 510(k) Applications for this Company
Contact	RON WARREN Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	FEQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/31/2010
Decision Date	09/13/2010
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