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FDA 510(k)

CX50 DIAGNOSTIC ULTRASOUND SYSTEM

K-Number: K111513 · 2011-06-24

Decision Date2011-06-24
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CX50 DIAGNOSTIC ULTRASOUND SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Philips Ultrasound, Inc.. It received FDA 510(k) clearance on 2011-06-24 under 510(k) number K111513. 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 CX50 DIAGNOSTIC ULTRASOUND SYSTEM?

CX50 DIAGNOSTIC ULTRASOUND SYSTEM is a medical device that received FDA 510(k) clearance on 2011-06-24. The listed applicant is Philips Ultrasound, Inc.. The 510(k) number is K111513.

When did CX50 DIAGNOSTIC ULTRASOUND SYSTEM receive FDA 510(k) clearance?

CX50 DIAGNOSTIC ULTRASOUND SYSTEM received FDA 510(k) clearance on 2011-06-24, under 510(k) number K111513.

Who is the listed applicant for CX50 DIAGNOSTIC ULTRASOUND SYSTEM?

The FDA 510(k) record lists Philips Ultrasound, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CX50 DIAGNOSTIC ULTRASOUND SYSTEM?

The FDA product code for CX50 DIAGNOSTIC ULTRASOUND SYSTEM is IYN.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Philips Ultrasound, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 43 devices →

Related Devices (Code: IYN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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