HDI 5000 DIAGNOSTIC ULTRASOUND SYSTEM
K-Number: K034003 · 2004-01-08
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Device Summary
Frequently Asked Questions
What is the HDI 5000 DIAGNOSTIC ULTRASOUND SYSTEM?
HDI 5000 DIAGNOSTIC ULTRASOUND SYSTEM is a medical device that received FDA 510(k) clearance on 2004-01-08. The listed applicant is Philips Ultrasound, Inc.. The 510(k) number is K034003.
When did HDI 5000 DIAGNOSTIC ULTRASOUND SYSTEM receive FDA 510(k) clearance?
HDI 5000 DIAGNOSTIC ULTRASOUND SYSTEM received FDA 510(k) clearance on 2004-01-08, under 510(k) number K034003.
Who is the listed applicant for HDI 5000 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 HDI 5000 DIAGNOSTIC ULTRASOUND SYSTEM?
The FDA product code for HDI 5000 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.
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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