510(k) K063876

MODULAR DISINFECTION SYSTEM (MDS) FOR ENDOSCOPE REPROCESSING by Medivators Reprocessing Systems — Product Code FEB

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 14, 2007
Date Received
December 29, 2006
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).