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FDA 510(k)

IPACS PRISM

K-Number: K030751 · 2003-05-29

ApplicantRealtimeimage, Inc.
Decision Date2003-05-29
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IPACS PRISM is the device name listed in this FDA 510(k) record. The listed applicant is Realtimeimage, Inc.. It received FDA 510(k) clearance on 2003-05-29 under 510(k) number K030751. 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 IPACS PRISM?

IPACS PRISM is a medical device that received FDA 510(k) clearance on 2003-05-29. The listed applicant is Realtimeimage, Inc.. The 510(k) number is K030751.

When did IPACS PRISM receive FDA 510(k) clearance?

IPACS PRISM received FDA 510(k) clearance on 2003-05-29, under 510(k) number K030751.

Who is the listed applicant for IPACS PRISM?

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

What is the FDA product code for IPACS PRISM?

The FDA product code for IPACS PRISM 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 Realtimeimage, Inc. 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.

K050298IPACS PRISM-5.0K042781IPACS CARDIOK041366IPACS ORTHO

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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