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FDA 510(k)

PROTOS SOFTWARE

K-Number: K040709 · 2004-04-28

ApplicantAktina Medical Physics Corp.
Decision Date2004-04-28
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PROTOS SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Aktina Medical Physics Corp.. It received FDA 510(k) clearance on 2004-04-28 under 510(k) number K040709. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROTOS SOFTWARE?

PROTOS SOFTWARE is a medical device that received FDA 510(k) clearance on 2004-04-28. The listed applicant is Aktina Medical Physics Corp.. The 510(k) number is K040709.

When did PROTOS SOFTWARE receive FDA 510(k) clearance?

PROTOS SOFTWARE received FDA 510(k) clearance on 2004-04-28, under 510(k) number K040709.

Who is the listed applicant for PROTOS SOFTWARE?

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

What is the FDA product code for PROTOS SOFTWARE?

The FDA product code for PROTOS SOFTWARE is IYE.

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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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