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FDA 510(k)

DIAGNOSTIC ULTRASOUND SYSTEM TYPE 3535

K-Number: K905198 · 1991-08-28

ApplicantBruel & Kjaer
Decision Date1991-08-28
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIAGNOSTIC ULTRASOUND SYSTEM TYPE 3535 is the device name listed in this FDA 510(k) record. The listed applicant is Bruel & Kjaer. It received FDA 510(k) clearance on 1991-08-28 under 510(k) number K905198. 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 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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