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FDA 510(k)

Pocket Ultrasound System (C10, C10TX, C10RL, C10RLpro)

K-Number: K241979 · 2024-08-22

ApplicantBeijing Konted Medical Technology Co.,Ltd
Decision Date2024-08-22
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Pocket Ultrasound System (C10, C10TX, C10RL, C10RLpro) is a medical device manufactured by Beijing Konted Medical Technology Co.,Ltd. It received FDA 510(k) clearance on 2024-08-22 under approval number K241979. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Pocket Ultrasound System (C10, C10TX, C10RL, C10RLpro)?

Pocket Ultrasound System (C10, C10TX, C10RL, C10RLpro) is a medical device that received FDA 510(k) clearance on 2024-08-22. It is manufactured by Beijing Konted Medical Technology Co.,Ltd. The 510(k) number is K241979.

When was Pocket Ultrasound System (C10, C10TX, C10RL, C10RLpro) approved by the FDA?

Pocket Ultrasound System (C10, C10TX, C10RL, C10RLpro) received FDA 510(k) clearance on 2024-08-22, under approval number K241979.

What company makes Pocket Ultrasound System (C10, C10TX, C10RL, C10RLpro)?

Pocket Ultrasound System (C10, C10TX, C10RL, C10RLpro) is manufactured by Beijing Konted Medical Technology Co.,Ltd.

What is the FDA product code for Pocket Ultrasound System (C10, C10TX, C10RL, C10RLpro)?

The FDA product code for Pocket Ultrasound System (C10, C10TX, C10RL, C10RLpro) is IYN.

Related Clinical Trials

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Related PubMed Literature

PMID: 37209414 Adverse events associated with Aveir Journal of cardiovascular electrophysiology (2023)

Other Devices by Beijing Konted Medical Technology Co.,Ltd

K231354Pocket Ultrasound System (C10)

Related Devices (Code: IYN)

K162845DC-40/DC-35/DC-45/DC-40S/DC-40 Pro Diagnostic Ultrasound SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd. K162902ARIETTA Prologue Diagnostic Ultrasound system and TransducersHitachi , Ltd. K163138Clarius Ultrasound SystemClarius Mobile Health Corp. K163077LOGIQ E9, LOGIQ E9 XDClear 2.0GE Medical Systems Ultrasound and Primary Care Diagnostics K162583ALOKA LISENDO 880Hitachi , Ltd. K163020Xperius Ultrasound SystemPhilips Health Care

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.

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