510(k) K192662

CapsoCam Plus (SV-3) Capsule Endoscopy System by CapsoVision, Inc. — Product Code NEZ

K192662 is an FDA 510(k) premarket notification submitted by CapsoVision, Inc. for the device "CapsoCam Plus (SV-3) Capsule Endoscopy System". The FDA issued a decision of Substantially Equivalent on February 14, 2020. The device falls under product code NEZ (System, Imaging, Gastrointestinal, Wireless, Capsule), a Class II device regulated under 21 CFR 876.1300. CapsoVision, Inc. has at least 5 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 14, 2020
Date Received
September 25, 2019
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Imaging, Gastrointestinal, Wireless, Capsule
Device Class
Class II
Regulation Number
876.1300
Review Panel
GU
Submission Type