Atlas FDA

NaviCam Xpress Stomach System, NaviCam Xpress System

FDA 510(k) clearance K230694 · decided 2023-04-13

Clearance details

K-number
K230694
Device name
NaviCam Xpress Stomach System, NaviCam Xpress System
Applicant
Anx Robotica Corp
Decision
Substantially Equivalent
Date received
2023-03-13
Decision date
2023-04-13
Days to decision
31 days
Clearance type
Special
Product code
QKZ
Device class
2
Regulation number
876.1310
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Plano, TX, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Stomach Capsule/Tether (NaviCam Xpress Stomach System with NaviCam Capsule/Tether) (K241934)Anx Robotica Corp2024-07-31
NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Capsule and NaviCam Tether (K231960)Anx Robotica Corporation2023-10-03
NaviCam Capsule Endoscope System with NaviCam Stomach Capsule and NaviCam Tether, NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Stomach Capsule and NaviCam Tether (K221608)Anx Robotica Corp2022-11-22
NaviCam Xpress Stomach System (K203192)Anx Robotica Corp2021-05-04
NaviCam Capsule Endoscope System with NaviCam Stomach Capsule (DEN190037)Anx Robotica, Inc.2020-05-22

Recalls involving this device

No recalls on record reference this clearance.