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FDA 510(k)

NERVEVISION SOFTWARE SYSTEMS

K-Number: K121075 · 2012-07-26

Applicant3D Imaging Partners, Inc.
Decision Date2012-07-26
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NERVEVISION SOFTWARE SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is 3D Imaging Partners, Inc.. It received FDA 510(k) clearance on 2012-07-26 under 510(k) number K121075. 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 NERVEVISION SOFTWARE SYSTEMS?

NERVEVISION SOFTWARE SYSTEMS is a medical device that received FDA 510(k) clearance on 2012-07-26. The listed applicant is 3D Imaging Partners, Inc.. The 510(k) number is K121075.

When did NERVEVISION SOFTWARE SYSTEMS receive FDA 510(k) clearance?

NERVEVISION SOFTWARE SYSTEMS received FDA 510(k) clearance on 2012-07-26, under 510(k) number K121075.

Who is the listed applicant for NERVEVISION SOFTWARE SYSTEMS?

The FDA 510(k) record lists 3D Imaging Partners, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NERVEVISION SOFTWARE SYSTEMS?

The FDA product code for NERVEVISION SOFTWARE SYSTEMS is LLZ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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