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FDA 510(k)

TIGRT TPS

K-Number: K090893 · 2009-07-15

ApplicantLinatech, LLC
Decision Date2009-07-15
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TIGRT TPS is the device name listed in this FDA 510(k) record. The listed applicant is Linatech, LLC. It received FDA 510(k) clearance on 2009-07-15 under 510(k) number K090893. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TIGRT TPS?

TIGRT TPS is a medical device that received FDA 510(k) clearance on 2009-07-15. The listed applicant is Linatech, LLC. The 510(k) number is K090893.

When did TIGRT TPS receive FDA 510(k) clearance?

TIGRT TPS received FDA 510(k) clearance on 2009-07-15, under 510(k) number K090893.

Who is the listed applicant for TIGRT TPS?

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

What is the FDA product code for TIGRT TPS?

The FDA product code for TIGRT TPS is MUJ.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Linatech, LLC 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.

K232489VenusXK092550TIGRT IVSK090802TIGRT MLC, TIGRT DMLC

Related Devices (Code: MUJ)

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.

K260750Virtual Cone (1.0)Varian Medical Systems, Inc.K253050RadOncAIInformaiK260207Multimodality Simulation Workspace (MM Sim) (v1.0.0)Philips Medical Systems Nederland B.V.K252784eXaSkin PlusAnatomical Geometry S.L.K253078ART.1-USSeetreat Pty, Ltd.K252304syngo.via RT Image Suite VC10Varian Medical Systems, Inc.

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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