510(k) K190969

ENDOSCOPE REPROCESSOR OER-Elite by Olympus Medical Systems Corp. — Product Code FEB

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 9, 2019
Date Received
April 12, 2019
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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

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).