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FDA 510(k)

MRP-7000: SUPPLEMENTAL R/F COILS

K-Number: K905835 · 1991-02-19

ApplicantSummit World Trade Corp.
Decision Date1991-02-19
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MRP-7000: SUPPLEMENTAL R/F COILS 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 1991-02-19 under 510(k) number K905835. 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 MRP-7000: SUPPLEMENTAL R/F COILS?

MRP-7000: SUPPLEMENTAL R/F COILS is a medical device that received FDA 510(k) clearance on 1991-02-19. The listed applicant is Summit World Trade Corp.. The 510(k) number is K905835.

When did MRP-7000: SUPPLEMENTAL R/F COILS receive FDA 510(k) clearance?

MRP-7000: SUPPLEMENTAL R/F COILS received FDA 510(k) clearance on 1991-02-19, under 510(k) number K905835.

Who is the listed applicant for MRP-7000: SUPPLEMENTAL R/F COILS?

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 MRP-7000: SUPPLEMENTAL R/F COILS?

The FDA product code for MRP-7000: SUPPLEMENTAL R/F COILS 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.

K905832MRP -5000(1): VERSION 2.0 SOFTWAREK905833MRP-5000(1): 2-D INFLOW MR ANGIOGRAPHYK905834MRP-7000(1) : 2-D INFLOW MR ANGIOGRAPHYK903318MAGNETIC RESONANCE DIAGNOSTIC DEVICE MOBILE MRP-30K903203MRP-20: HS/MR HEAD COIL 3-D FT RECONSTRUCTIONK903204MRP-20: SUPPL R/F COIL HS/MR QUADRATURE HEAD COIL

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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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