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FDA 510(k)

VICTOREEN THEBES II, MODEL 7020

K-Number: K024284 · 2003-03-11

ApplicantSyncor Radiation Management
Decision Date2003-03-11
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VICTOREEN THEBES II, MODEL 7020 is the device name listed in this FDA 510(k) record. The listed applicant is Syncor Radiation Management. It received FDA 510(k) clearance on 2003-03-11 under 510(k) number K024284. 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 VICTOREEN THEBES II, MODEL 7020?

VICTOREEN THEBES II, MODEL 7020 is a medical device that received FDA 510(k) clearance on 2003-03-11. The listed applicant is Syncor Radiation Management. The 510(k) number is K024284.

When did VICTOREEN THEBES II, MODEL 7020 receive FDA 510(k) clearance?

VICTOREEN THEBES II, MODEL 7020 received FDA 510(k) clearance on 2003-03-11, under 510(k) number K024284.

Who is the listed applicant for VICTOREEN THEBES II, MODEL 7020?

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

What is the FDA product code for VICTOREEN THEBES II, MODEL 7020?

The FDA product code for VICTOREEN THEBES II, MODEL 7020 is IYE.

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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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