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FDA 510(k)

UD 2000 VIDEO OPTION

K-Number: K915342 · 1992-06-10

ApplicantDiagnostic Ultrasound Corp.
Decision Date1992-06-10
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

UD 2000 VIDEO OPTION is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Ultrasound Corp.. It received FDA 510(k) clearance on 1992-06-10 under 510(k) number K915342. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UD 2000 VIDEO OPTION?

UD 2000 VIDEO OPTION is a medical device that received FDA 510(k) clearance on 1992-06-10. The listed applicant is Diagnostic Ultrasound Corp.. The 510(k) number is K915342.

When did UD 2000 VIDEO OPTION receive FDA 510(k) clearance?

UD 2000 VIDEO OPTION received FDA 510(k) clearance on 1992-06-10, under 510(k) number K915342.

Who is the listed applicant for UD 2000 VIDEO OPTION?

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

What is the FDA product code for UD 2000 VIDEO OPTION?

The FDA product code for UD 2000 VIDEO OPTION is LLZ.

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Other records listing Diagnostic Ultrasound Corp. 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.

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Related Devices (Code: LLZ)

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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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