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)

MAGNETIC RESONANCE DIAGNOSTIC DEVICE(ACCESORY)

K-Number: K915567 · 1992-05-15

ApplicantFonar Corp.
Decision Date1992-05-15
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAGNETIC RESONANCE DIAGNOSTIC DEVICE(ACCESORY) is the device name listed in this FDA 510(k) record. The listed applicant is Fonar Corp.. It received FDA 510(k) clearance on 1992-05-15 under 510(k) number K915567. 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 MAGNETIC RESONANCE DIAGNOSTIC DEVICE(ACCESORY)?

MAGNETIC RESONANCE DIAGNOSTIC DEVICE(ACCESORY) is a medical device that received FDA 510(k) clearance on 1992-05-15. The listed applicant is Fonar Corp.. The 510(k) number is K915567.

When did MAGNETIC RESONANCE DIAGNOSTIC DEVICE(ACCESORY) receive FDA 510(k) clearance?

MAGNETIC RESONANCE DIAGNOSTIC DEVICE(ACCESORY) received FDA 510(k) clearance on 1992-05-15, under 510(k) number K915567.

Who is the listed applicant for MAGNETIC RESONANCE DIAGNOSTIC DEVICE(ACCESORY)?

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

What is the FDA product code for MAGNETIC RESONANCE DIAGNOSTIC DEVICE(ACCESORY)?

The FDA product code for MAGNETIC RESONANCE DIAGNOSTIC DEVICE(ACCESORY) 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 Fonar Corp. 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.

K061930INDOMITABLE MAGNETIC RESONANCE IMAGING SCANNER ACCESSORYK011485PINNACLE MAGNETIC RESONANCE IMAGING SCANNERK003453SYMPULSE COMPUTER SYSTEM FOR FONAR MRI SCANNERSK002490INDOMITABLE MAGNETIC RESONANCE IMAGING SCANNERK994287FONAR 360 DEGREE MAGNETIC RESONANCE IMAGING SCANNERK951681QUAD 1200 MAGNETIC RESONANCE IMAGING SCANNER

View all 12 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.

↑