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FDA 510(k)

MOBILE MRP-20 MAGNETIC RESONANCE DIAGNOSTIC DEVICE

K-Number: K901980 · 1990-06-28

ApplicantSummit World Trade Corp.
Decision Date1990-06-28
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MOBILE MRP-20 MAGNETIC RESONANCE DIAGNOSTIC DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Summit World Trade Corp.. It received FDA 510(k) clearance on 1990-06-28 under 510(k) number K901980. 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 MOBILE MRP-20 MAGNETIC RESONANCE DIAGNOSTIC DEVICE?

MOBILE MRP-20 MAGNETIC RESONANCE DIAGNOSTIC DEVICE is a medical device that received FDA 510(k) clearance on 1990-06-28. The listed applicant is Summit World Trade Corp.. The 510(k) number is K901980.

When did MOBILE MRP-20 MAGNETIC RESONANCE DIAGNOSTIC DEVICE receive FDA 510(k) clearance?

MOBILE MRP-20 MAGNETIC RESONANCE DIAGNOSTIC DEVICE received FDA 510(k) clearance on 1990-06-28, under 510(k) number K901980.

Who is the listed applicant for MOBILE MRP-20 MAGNETIC RESONANCE DIAGNOSTIC DEVICE?

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

What is the FDA product code for MOBILE MRP-20 MAGNETIC RESONANCE DIAGNOSTIC DEVICE?

The FDA product code for MOBILE MRP-20 MAGNETIC RESONANCE DIAGNOSTIC DEVICE is LNH.

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Other records listing Summit World Trade 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.

K905833MRP-5000(1): 2-D INFLOW MR ANGIOGRAPHYK905832MRP -5000(1): VERSION 2.0 SOFTWAREK905835MRP-7000: SUPPLEMENTAL R/F COILSK905834MRP-7000(1) : 2-D INFLOW MR ANGIOGRAPHYK903318MAGNETIC RESONANCE DIAGNOSTIC DEVICE MOBILE MRP-30K903203MRP-20: HS/MR HEAD COIL 3-D FT RECONSTRUCTION

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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.

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