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FDA 510(k)

DIVO

K-Number: K072637 · 2007-12-11

ApplicantA2d Imaging, LLC
Decision Date2007-12-11
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIVO is the device name listed in this FDA 510(k) record. The listed applicant is A2d Imaging, LLC. It received FDA 510(k) clearance on 2007-12-11 under 510(k) number K072637. 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 DIVO?

DIVO is a medical device that received FDA 510(k) clearance on 2007-12-11. The listed applicant is A2d Imaging, LLC. The 510(k) number is K072637.

When did DIVO receive FDA 510(k) clearance?

DIVO received FDA 510(k) clearance on 2007-12-11, under 510(k) number K072637.

Who is the listed applicant for DIVO?

The FDA 510(k) record lists A2d Imaging, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIVO?

The FDA product code for DIVO is LLZ.

Related Devices (Code: LLZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261874Syneris PACS v.1.0.1.0SynerisK262442HipStudio AnalysisReplasia BVK261855Elucid PlaqueIQElucid Bioimaging, Inc.K254214OOOPDSTaiwan Main Orthopaedic Biotechnology Co., Ltd.K261861SPINEsim v1.0Mdsim S.A.K2620603D-RD-SRadiopharmaceutical Imaging & Dosimetry, LLC

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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