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)

MAGNA SL

K-Number: K940894 · 1994-09-02

ApplicantMagna-Lab, Inc.
Decision Date1994-09-02
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAGNA SL is the device name listed in this FDA 510(k) record. The listed applicant is Magna-Lab, Inc.. It received FDA 510(k) clearance on 1994-09-02 under 510(k) number K940894. 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 MAGNA SL?

MAGNA SL is a medical device that received FDA 510(k) clearance on 1994-09-02. The listed applicant is Magna-Lab, Inc.. The 510(k) number is K940894.

When did MAGNA SL receive FDA 510(k) clearance?

MAGNA SL received FDA 510(k) clearance on 1994-09-02, under 510(k) number K940894.

Who is the listed applicant for MAGNA SL?

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

What is the FDA product code for MAGNA SL?

The FDA product code for MAGNA SL 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 Magna-Lab, 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.

K020993ILLUMINATOR AUTOMATIC TUNE VOX AND INTERFACE CABLE (ATIB)K010802CARDIAC VIEW, MODEL 2001K010513CARDIAC VIEW, MODEL 2001

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.

↑