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FDA 510(k)

3DNET SUITE

K-Number: K063107 · 2006-10-27

ApplicantBiotronics3D, Ltd.
Decision Date2006-10-27
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

3DNET SUITE is the device name listed in this FDA 510(k) record. The listed applicant is Biotronics3D, Ltd.. It received FDA 510(k) clearance on 2006-10-27 under 510(k) number K063107. 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 3DNET SUITE?

3DNET SUITE is a medical device that received FDA 510(k) clearance on 2006-10-27. The listed applicant is Biotronics3D, Ltd.. The 510(k) number is K063107.

When did 3DNET SUITE receive FDA 510(k) clearance?

3DNET SUITE received FDA 510(k) clearance on 2006-10-27, under 510(k) number K063107.

Who is the listed applicant for 3DNET SUITE?

The FDA 510(k) record lists Biotronics3D, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3DNET SUITE?

The FDA product code for 3DNET SUITE 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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