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FDA 510(k)

ACCESS MAGNETIC RESONANCE DEVICE ACCESSORY

K-Number: K930960 · 1993-11-01

ApplicantToshiba America Mri, Inc.
Decision Date1993-11-01
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ACCESS MAGNETIC RESONANCE DEVICE ACCESSORY is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba America Mri, Inc.. It received FDA 510(k) clearance on 1993-11-01 under 510(k) number K930960. 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 ACCESS MAGNETIC RESONANCE DEVICE ACCESSORY?

ACCESS MAGNETIC RESONANCE DEVICE ACCESSORY is a medical device that received FDA 510(k) clearance on 1993-11-01. The listed applicant is Toshiba America Mri, Inc.. The 510(k) number is K930960.

When did ACCESS MAGNETIC RESONANCE DEVICE ACCESSORY receive FDA 510(k) clearance?

ACCESS MAGNETIC RESONANCE DEVICE ACCESSORY received FDA 510(k) clearance on 1993-11-01, under 510(k) number K930960.

Who is the listed applicant for ACCESS MAGNETIC RESONANCE DEVICE ACCESSORY?

The FDA 510(k) record lists Toshiba America Mri, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACCESS MAGNETIC RESONANCE DEVICE ACCESSORY?

The FDA product code for ACCESS MAGNETIC RESONANCE DEVICE ACCESSORY is LNH.

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Other records listing Toshiba America Mri, 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.

K002531EXCELART WITH PIANISSIMO, MODEL MRT-1501/P3K002522OPART, MODEL MRT-600K000549OPART, MODEL MRT-600K993803EXCELART WITH PIANISSIMOK993574OPART/PRODIGA, OPART/PROTENZA, OPART/PARAGONK991740OPART, MODEL MRT-600

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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.

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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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