510(k) K191282

PENTAX Medical EPK-i7010 and PENTAX EPK-i5010 Video Processors with GI Family by Pentax of America, Inc. — Product Code PEA

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 8, 2019
Date Received
May 13, 2019
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Endoscope, Accessories, Image Post-Processing For Color Enhancement
Device Class
Class II
Regulation Number
876.1500
Review Panel
GU
Submission Type

Alternative mode of visualization using image post-processing algorithms of the received white light image for color enhancement.