510(k) K200989

Reliance Endoscope Processing System by STERIS Corporation — Product Code NZA

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 14, 2020
Date Received
April 15, 2020
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Accessories, Germicide, Cleaning, For Endoscopes
Device Class
Class II
Regulation Number
876.1500
Review Panel
HO
Submission Type

High level disinfection of reusable, heat-sensitive devices If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).