FDA 510(k) Application Details - K100237

Device Classification Name	Meter, Conductivity, Induction, Remote Type   More FDA Info for this Device
510(K) Number	K100237
Device Name	Meter, Conductivity, Induction, Remote Type
Applicant	MYRON L COMPANY 2450 IMPALA DR. CARLSBAD, CA 92010-7226 US Other 510(k) Applications for this Company
Contact	RICHARD JAMES SPAHL Other 510(k) Applications for this Contact
Regulation Number	876.5820   More FDA Info for this Regulation Number
Classification Product Code	FLB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/26/2010
Decision Date	04/23/2010
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