CapsoCam Plus (SV-3) Capsule Endoscopy System
K-Number: K192662 · 2020-02-14
Device Summary
Frequently Asked Questions
What is the CapsoCam Plus (SV-3) Capsule Endoscopy System?
CapsoCam Plus (SV-3) Capsule Endoscopy System is a medical device that received FDA 510(k) clearance on 2020-02-14. It is manufactured by CapsoVision, Inc.. The 510(k) number is K192662.
When was CapsoCam Plus (SV-3) Capsule Endoscopy System approved by the FDA?
CapsoCam Plus (SV-3) Capsule Endoscopy System received FDA 510(k) clearance on 2020-02-14, under approval number K192662.
What company makes CapsoCam Plus (SV-3) Capsule Endoscopy System?
CapsoCam Plus (SV-3) Capsule Endoscopy System is manufactured by CapsoVision, Inc..
What is the FDA product code for CapsoCam Plus (SV-3) Capsule Endoscopy System?
The FDA product code for CapsoCam Plus (SV-3) Capsule Endoscopy System is NEZ.
Related Clinical Trials
Other Devices by CapsoVision, Inc.
Related Devices (Code: NEZ)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.