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FDA 510(k)

ACUSON P500 Ultrasound System; ACUSON P500 ICE Ultrasound System

K-Number: K233610 · 2024-06-12

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2024-06-12
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ACUSON P500 Ultrasound System; ACUSON P500 ICE Ultrasound System is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2024-06-12 under approval number K233610. 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 ACUSON P500 Ultrasound System; ACUSON P500 ICE Ultrasound System?

ACUSON P500 Ultrasound System; ACUSON P500 ICE Ultrasound System is a medical device that received FDA 510(k) clearance on 2024-06-12. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K233610.

When was ACUSON P500 Ultrasound System; ACUSON P500 ICE Ultrasound System approved by the FDA?

ACUSON P500 Ultrasound System; ACUSON P500 ICE Ultrasound System received FDA 510(k) clearance on 2024-06-12, under approval number K233610.

What company makes ACUSON P500 Ultrasound System; ACUSON P500 ICE Ultrasound System?

ACUSON P500 Ultrasound System; ACUSON P500 ICE Ultrasound System is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for ACUSON P500 Ultrasound System; ACUSON P500 ICE Ultrasound System?

The FDA product code for ACUSON P500 Ultrasound System; ACUSON P500 ICE Ultrasound System is IYN.

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Related Devices (Code: IYN)

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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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