FDA 510(k)

ULTRAPROBE

K-Number: K810133 · 1981-06-09

Decision Date1981-06-09

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

ULTRAPROBE is the device name listed in this FDA 510(k) record. The listed applicant is Ars Magna. It received FDA 510(k) clearance on 1981-06-09 under 510(k) number K810133. 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 ULTRAPROBE?

ULTRAPROBE is a medical device that received FDA 510(k) clearance on 1981-06-09. The listed applicant is Ars Magna. The 510(k) number is K810133.

When did ULTRAPROBE receive FDA 510(k) clearance?

ULTRAPROBE received FDA 510(k) clearance on 1981-06-09, under 510(k) number K810133.

Who is the listed applicant for ULTRAPROBE?

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

What is the FDA product code for ULTRAPROBE?

The FDA product code for ULTRAPROBE is IYN.

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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.