FDA 510(k) Application Details - K122362

Device Classification Name	Indicator, Biological Sterilization Process   More FDA Info for this Device
510(K) Number	K122362
Device Name	Indicator, Biological Sterilization Process
Applicant	MESA LABORATORIES, INC. 12100 W. 6TH AVENUE LAKEWOOD, CO 80228 US Other 510(k) Applications for this Company
Contact	JOLE WILSON Other 510(k) Applications for this Contact
Regulation Number	880.2800   More FDA Info for this Regulation Number
Classification Product Code	FRC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/06/2012
Decision Date	03/26/2013
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review