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FDA 510(k)

MIRAGE

K-Number: K972886 · 1997-10-01

ApplicantSegami Corp., Inc.
Decision Date1997-10-01
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MIRAGE is the device name listed in this FDA 510(k) record. The listed applicant is Segami Corp., Inc.. It received FDA 510(k) clearance on 1997-10-01 under 510(k) number K972886. 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 MIRAGE?

MIRAGE is a medical device that received FDA 510(k) clearance on 1997-10-01. The listed applicant is Segami Corp., Inc.. The 510(k) number is K972886.

When did MIRAGE receive FDA 510(k) clearance?

MIRAGE received FDA 510(k) clearance on 1997-10-01, under 510(k) number K972886.

Who is the listed applicant for MIRAGE?

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

What is the FDA product code for MIRAGE?

The FDA product code for MIRAGE 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 Segami Corp., 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.

K010726MODIFICATION TO MIRAGE

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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