DIAGNOSTIC ULTRASOUND SYSTEM TYPE 3535
K-Number: K905198 · 1991-08-28
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Device Summary
Frequently Asked Questions
What is the DIAGNOSTIC ULTRASOUND SYSTEM TYPE 3535?
DIAGNOSTIC ULTRASOUND SYSTEM TYPE 3535 is a medical device that received FDA 510(k) clearance on 1991-08-28. The listed applicant is Bruel & Kjaer. The 510(k) number is K905198.
When did DIAGNOSTIC ULTRASOUND SYSTEM TYPE 3535 receive FDA 510(k) clearance?
DIAGNOSTIC ULTRASOUND SYSTEM TYPE 3535 received FDA 510(k) clearance on 1991-08-28, under 510(k) number K905198.
Who is the listed applicant for DIAGNOSTIC ULTRASOUND SYSTEM TYPE 3535?
The FDA 510(k) record lists Bruel & Kjaer as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIAGNOSTIC ULTRASOUND SYSTEM TYPE 3535?
The FDA product code for DIAGNOSTIC ULTRASOUND SYSTEM TYPE 3535 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 Bruel & Kjaer 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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