FDA 510(k)

MODEIFICATION TO IPLAN RT DOSE

K-Number: K080888 · 2008-06-11

Decision Date2008-06-11

Product CodeMUJ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MODEIFICATION TO IPLAN RT DOSE is the device name listed in this FDA 510(k) record. The listed applicant is Brainlab AG. It received FDA 510(k) clearance on 2008-06-11 under 510(k) number K080888. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEIFICATION TO IPLAN RT DOSE?

MODEIFICATION TO IPLAN RT DOSE is a medical device that received FDA 510(k) clearance on 2008-06-11. The listed applicant is Brainlab AG. The 510(k) number is K080888.

When did MODEIFICATION TO IPLAN RT DOSE receive FDA 510(k) clearance?

MODEIFICATION TO IPLAN RT DOSE received FDA 510(k) clearance on 2008-06-11, under 510(k) number K080888.

Who is the listed applicant for MODEIFICATION TO IPLAN RT DOSE?

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

What is the FDA product code for MODEIFICATION TO IPLAN RT DOSE?

The FDA product code for MODEIFICATION TO IPLAN RT DOSE is MUJ.

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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.