FDA 510(k)

VECTORVISION CRANIAL/ENT

K-Number: K023651 · 2004-02-17

Decision Date2004-02-17

Product CodeHAW

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

VECTORVISION CRANIAL/ENT is the device name listed in this FDA 510(k) record. The listed applicant is Brainlab AG. It received FDA 510(k) clearance on 2004-02-17 under 510(k) number K023651. 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 CRANIAL/ENT?

VECTORVISION CRANIAL/ENT is a medical device that received FDA 510(k) clearance on 2004-02-17. The listed applicant is Brainlab AG. The 510(k) number is K023651.

When did VECTORVISION CRANIAL/ENT receive FDA 510(k) clearance?

VECTORVISION CRANIAL/ENT received FDA 510(k) clearance on 2004-02-17, under 510(k) number K023651.

Who is the listed applicant for VECTORVISION CRANIAL/ENT?

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 CRANIAL/ENT?

The FDA product code for VECTORVISION CRANIAL/ENT 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.