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FDA 510(k)

DIASUS

K-Number: K013142 · 2001-10-05

ApplicantDynamic Imaging , Ltd.
Decision Date2001-10-05
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIASUS is the device name listed in this FDA 510(k) record. The listed applicant is Dynamic Imaging , Ltd.. It received FDA 510(k) clearance on 2001-10-05 under 510(k) number K013142. 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 DIASUS?

DIASUS is a medical device that received FDA 510(k) clearance on 2001-10-05. The listed applicant is Dynamic Imaging , Ltd.. The 510(k) number is K013142.

When did DIASUS receive FDA 510(k) clearance?

DIASUS received FDA 510(k) clearance on 2001-10-05, under 510(k) number K013142.

Who is the listed applicant for DIASUS?

The FDA 510(k) record lists Dynamic Imaging , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIASUS?

The FDA product code for DIASUS is IYO.

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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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