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FDA 510(k)

Ultrasound System 2300

K-Number: K222441 · 2022-12-07

ApplicantBk Medical Aps
Decision Date2022-12-07
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Ultrasound System 2300 is a medical device manufactured by Bk Medical Aps. It received FDA 510(k) clearance on 2022-12-07 under approval number K222441. 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 Ultrasound System 2300?

Ultrasound System 2300 is a medical device that received FDA 510(k) clearance on 2022-12-07. It is manufactured by Bk Medical Aps. The 510(k) number is K222441.

When was Ultrasound System 2300 approved by the FDA?

Ultrasound System 2300 received FDA 510(k) clearance on 2022-12-07, under approval number K222441.

What company makes Ultrasound System 2300?

Ultrasound System 2300 is manufactured by Bk Medical Aps.

What is the FDA product code for Ultrasound System 2300?

The FDA product code for Ultrasound System 2300 is IYN.

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Other Devices by Bk Medical Aps

K161960bk2300 K180737Ultrasound Scanner System bk2300 K173569Ultrasound System 1300 K231764Ultrasound System 1300 K223830Ultrasound System 2300

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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