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FDA 510(k)

PATXFER RT

K-Number: K040931 · 2004-07-22

ApplicantBrainlab AG
Decision Date2004-07-22
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PATXFER RT is the device name listed in this FDA 510(k) record. The listed applicant is Brainlab AG. It received FDA 510(k) clearance on 2004-07-22 under 510(k) number K040931. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATXFER RT?

PATXFER RT is a medical device that received FDA 510(k) clearance on 2004-07-22. The listed applicant is Brainlab AG. The 510(k) number is K040931.

When did PATXFER RT receive FDA 510(k) clearance?

PATXFER RT received FDA 510(k) clearance on 2004-07-22, under 510(k) number K040931.

Who is the listed applicant for PATXFER RT?

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 PATXFER RT?

The FDA product code for PATXFER RT is LLZ.

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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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