Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MAGNETOM SYSTEMS - I-CLASS AND T-CLASS RELEASES

K-Number: K062454 · 2006-11-03

ApplicantSiemens Medi Cal Solutions, Inc.
Decision Date2006-11-03
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAGNETOM SYSTEMS - I-CLASS AND T-CLASS RELEASES is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medi Cal Solutions, Inc.. It received FDA 510(k) clearance on 2006-11-03 under 510(k) number K062454. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGNETOM SYSTEMS - I-CLASS AND T-CLASS RELEASES?

MAGNETOM SYSTEMS - I-CLASS AND T-CLASS RELEASES is a medical device that received FDA 510(k) clearance on 2006-11-03. The listed applicant is Siemens Medi Cal Solutions, Inc.. The 510(k) number is K062454.

When did MAGNETOM SYSTEMS - I-CLASS AND T-CLASS RELEASES receive FDA 510(k) clearance?

MAGNETOM SYSTEMS - I-CLASS AND T-CLASS RELEASES received FDA 510(k) clearance on 2006-11-03, under 510(k) number K062454.

Who is the listed applicant for MAGNETOM SYSTEMS - I-CLASS AND T-CLASS RELEASES?

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

What is the FDA product code for MAGNETOM SYSTEMS - I-CLASS AND T-CLASS RELEASES?

The FDA product code for MAGNETOM SYSTEMS - I-CLASS AND T-CLASS RELEASES is LNH.

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 Siemens Medi Cal Solutions, 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.

K193216syngo.CT Lung CADK182639MOBILETT Elara MaxK182517MULTIX ImpactK181279Ysio MaxK173639Luminos dRF Max, Luminos Agile Max, Uroskop Omnia Max, Multitom RaxK173408Mammomat Revelation

View all 26 devices →

Related Devices (Code: LNH)

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.

K261758Embrace Vision Neonatal MRI SystemAspect Imaging, Ltd.K261283APERTO Lucent MRI SystemFujifilm CorporationK260758MAGNETOM Free.Max; MAGNETOM Free.StarSiemens Shenzhen Magnetic Resonance , Ltd.K262622Swoop® Portable MR Imaging® SystemHyperfine, Inc.K254250MagicScan-1.5, GreenMR Serenity 1.5TXingaoyi Medical Equipment Co.,LtdK253808AIR Recon DLGE Medical Systems

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.

↑