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)

ADD'L OPTIONS 1.5 TESLA & 1.0 TESLA TO MAGNETOM 42

K-Number: K895221 · 1989-10-03

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1989-10-03
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ADD'L OPTIONS 1.5 TESLA & 1.0 TESLA TO MAGNETOM 42 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1989-10-03 under 510(k) number K895221. 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 ADD'L OPTIONS 1.5 TESLA & 1.0 TESLA TO MAGNETOM 42?

ADD'L OPTIONS 1.5 TESLA & 1.0 TESLA TO MAGNETOM 42 is a medical device that received FDA 510(k) clearance on 1989-10-03. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K895221.

When did ADD'L OPTIONS 1.5 TESLA & 1.0 TESLA TO MAGNETOM 42 receive FDA 510(k) clearance?

ADD'L OPTIONS 1.5 TESLA & 1.0 TESLA TO MAGNETOM 42 received FDA 510(k) clearance on 1989-10-03, under 510(k) number K895221.

Who is the listed applicant for ADD'L OPTIONS 1.5 TESLA & 1.0 TESLA TO MAGNETOM 42?

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

What is the FDA product code for ADD'L OPTIONS 1.5 TESLA & 1.0 TESLA TO MAGNETOM 42?

The FDA product code for ADD'L OPTIONS 1.5 TESLA & 1.0 TESLA TO MAGNETOM 42 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 Medical Solutions USA, 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.

K260055syngo.CT Brain QuantificationK261696ACUNAV Luxera 4D ICE CatheterK260488MULTIX Impact; MULTIX Impact CK253786syngo.CT Coronary CockpitK253678MAMMOMAT B.brilliant (11372950)K260844ACUSON Sequoia Diagnostic Ultrasound System;ACUSON Sequoia Select Diagnostic Ultrasound System;ACUSON Origin Diagnostic Ultrasound System;ACUSON Origin ICE Diagnostic Ultrasound System

View all 732 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.

↑