FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CapsoCam Plus (SV-3) Capsule Endoscopy System

K Number: K192662 · Decision Feb 14, 2020
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
46
Applicant Total
6
Review Days
142

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Basic Information

Device Name
CapsoCam Plus (SV-3) Capsule Endoscopy System
K Number
K192662
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1300
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CapsoVision, Inc.
Date Received
September 25, 2019
Decision Date
February 14, 2020
Product Code
NEZ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NEZ System, Imaging, Gastrointestinal, Wireless, Capsule

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NEZ), ordered by most recent decision date.

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Other Clearances by CapsoVision, Inc.

K Number Device Name
K252480 CE Deliver (DLV)
K242643 CapsoCam Plus (SV-3) Capsule Endoscopy System
K183192 CapsoCam Plus (SV-3)
K161773 CapsoCam Plus (SV-3) Capsule Endoscope System
K151635 CapsoCam (SV-1)