510(k) K171587

VERIFY Incubator for Assert VH2O2 Self-Contained Biological Indicator by STERIS Corporation — Product Code FRC

K171587 is an FDA 510(k) premarket notification submitted by STERIS Corporation for the device "VERIFY Incubator for Assert VH2O2 Self-Contained Biological Indicator". The FDA issued a decision of Substantially Equivalent on Aug 22, 2017. The device falls under product code FRC (Indicator, Biological Sterilization Process), a Class II device regulated under 21 CFR 880.2800. STERIS Corporation has 204 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Aug 22, 2017
Date Received
May 31, 2017
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Indicator, Biological Sterilization Process
Device Class
Class II
Regulation Number
880.2800
Review Panel
HO
Submission Type
510(k)