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FDA 510(k)

ORTHOPACS

K-Number: K033825 · 2004-02-02

ApplicantEtrauma.Com Corp.
Decision Date2004-02-02
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ORTHOPACS is the device name listed in this FDA 510(k) record. The listed applicant is Etrauma.Com Corp.. It received FDA 510(k) clearance on 2004-02-02 under 510(k) number K033825. 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 ORTHOPACS?

ORTHOPACS is a medical device that received FDA 510(k) clearance on 2004-02-02. The listed applicant is Etrauma.Com Corp.. The 510(k) number is K033825.

When did ORTHOPACS receive FDA 510(k) clearance?

ORTHOPACS received FDA 510(k) clearance on 2004-02-02, under 510(k) number K033825.

Who is the listed applicant for ORTHOPACS?

The FDA 510(k) record lists Etrauma.Com Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ORTHOPACS?

The FDA product code for ORTHOPACS is LLZ.

Related Clinical Trials

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.

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Other records listing Etrauma.Com Corp. as applicant

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.

K994228REMOTEIMAGE SYSTEM

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

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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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