AU5 ULTRASOUND IMAGING SYSTEM
K-Number: K980468 · 1998-08-26
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Device Summary
Frequently Asked Questions
What is the AU5 ULTRASOUND IMAGING SYSTEM?
AU5 ULTRASOUND IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 1998-08-26. The listed applicant is Biosound Esaote, Inc.. The 510(k) number is K980468.
When did AU5 ULTRASOUND IMAGING SYSTEM receive FDA 510(k) clearance?
AU5 ULTRASOUND IMAGING SYSTEM received FDA 510(k) clearance on 1998-08-26, under 510(k) number K980468.
Who is the listed applicant for AU5 ULTRASOUND IMAGING SYSTEM?
The FDA 510(k) record lists Biosound Esaote, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AU5 ULTRASOUND IMAGING SYSTEM?
The FDA product code for AU5 ULTRASOUND IMAGING 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 Biosound Esaote, 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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