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FDA 510(k)

UD-1000 ULTRASONIC A/B SCANNER

K-Number: K020151 · 2002-04-10

ApplicantTomey Corp. USA
Decision Date2002-04-10
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

UD-1000 ULTRASONIC A/B SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Tomey Corp. USA. It received FDA 510(k) clearance on 2002-04-10 under 510(k) number K020151. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UD-1000 ULTRASONIC A/B SCANNER?

UD-1000 ULTRASONIC A/B SCANNER is a medical device that received FDA 510(k) clearance on 2002-04-10. The listed applicant is Tomey Corp. USA. The 510(k) number is K020151.

When did UD-1000 ULTRASONIC A/B SCANNER receive FDA 510(k) clearance?

UD-1000 ULTRASONIC A/B SCANNER received FDA 510(k) clearance on 2002-04-10, under 510(k) number K020151.

Who is the listed applicant for UD-1000 ULTRASONIC A/B SCANNER?

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

What is the FDA product code for UD-1000 ULTRASONIC A/B SCANNER?

The FDA product code for UD-1000 ULTRASONIC A/B SCANNER is IYO.

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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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