FDA 510(k)

@ TARGET

K-Number: K983410 · 1999-09-17

Decision Date1999-09-17

Product CodeHAW

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

@ TARGET is the device name listed in this FDA 510(k) record. The listed applicant is Brainlab AG. It received FDA 510(k) clearance on 1999-09-17 under 510(k) number K983410. 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 @ TARGET?

@ TARGET is a medical device that received FDA 510(k) clearance on 1999-09-17. The listed applicant is Brainlab AG. The 510(k) number is K983410.

When did @ TARGET receive FDA 510(k) clearance?

@ TARGET received FDA 510(k) clearance on 1999-09-17, under 510(k) number K983410.

Who is the listed applicant for @ TARGET?

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 @ TARGET?

The FDA product code for @ TARGET is HAW.

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Other records listing Brainlab AG as applicant

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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.