FDA 510(k) Application Details - K212424

Device Classification Name	Sterilizer, Steam   More FDA Info for this Device
510(K) Number	K212424
Device Name	Sterilizer, Steam
Applicant	STERIS Corporation 5960 Heisley Rd Mentor, OH 44060 US Other 510(k) Applications for this Company
Contact	Anthony Piotrkowski Other 510(k) Applications for this Contact
Regulation Number	880.6880   More FDA Info for this Regulation Number
Classification Product Code	FLE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/04/2021
Decision Date	10/28/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review