FDA 510(k)

VECTORVISION FLUORO3D

K-Number: K024192 · 2003-06-11

Decision Date2003-06-11

Product CodeHAW

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

VECTORVISION FLUORO3D is the device name listed in this FDA 510(k) record. The listed applicant is Brainlab AG. It received FDA 510(k) clearance on 2003-06-11 under 510(k) number K024192. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VECTORVISION FLUORO3D?

VECTORVISION FLUORO3D is a medical device that received FDA 510(k) clearance on 2003-06-11. The listed applicant is Brainlab AG. The 510(k) number is K024192.

When did VECTORVISION FLUORO3D receive FDA 510(k) clearance?

VECTORVISION FLUORO3D received FDA 510(k) clearance on 2003-06-11, under 510(k) number K024192.

Who is the listed applicant for VECTORVISION FLUORO3D?

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 VECTORVISION FLUORO3D?

The FDA product code for VECTORVISION FLUORO3D is HAW.

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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.