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FDA 510(k)

MODIFIED HITACHI MRP-20 MAGNETIC RESONANCE DIAGNOS

K-Number: K900919 · 1990-05-14

ApplicantSummit World Trade Corp.
Decision Date1990-05-14
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODIFIED HITACHI MRP-20 MAGNETIC RESONANCE DIAGNOS 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 1990-05-14 under 510(k) number K900919. 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 MODIFIED HITACHI MRP-20 MAGNETIC RESONANCE DIAGNOS?

MODIFIED HITACHI MRP-20 MAGNETIC RESONANCE DIAGNOS is a medical device that received FDA 510(k) clearance on 1990-05-14. The listed applicant is Summit World Trade Corp.. The 510(k) number is K900919.

When did MODIFIED HITACHI MRP-20 MAGNETIC RESONANCE DIAGNOS receive FDA 510(k) clearance?

MODIFIED HITACHI MRP-20 MAGNETIC RESONANCE DIAGNOS received FDA 510(k) clearance on 1990-05-14, under 510(k) number K900919.

Who is the listed applicant for MODIFIED HITACHI MRP-20 MAGNETIC RESONANCE DIAGNOS?

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 MODIFIED HITACHI MRP-20 MAGNETIC RESONANCE DIAGNOS?

The FDA product code for MODIFIED HITACHI MRP-20 MAGNETIC RESONANCE DIAGNOS 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)

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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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