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FDA 510(k)

MAGNETIC RESONANCE DEVICE ACCESSORY

K-Number: K911276 · 1991-06-28

ApplicantToshiba America Mri, Inc.
Decision Date1991-06-28
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

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 1991-06-28 under 510(k) number K911276. 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 DEVICE ACCESSORY?

MAGNETIC RESONANCE DEVICE ACCESSORY is a medical device that received FDA 510(k) clearance on 1991-06-28. The listed applicant is Toshiba America Mri, Inc.. The 510(k) number is K911276.

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

MAGNETIC RESONANCE DEVICE ACCESSORY received FDA 510(k) clearance on 1991-06-28, under 510(k) number K911276.

Who is the listed applicant for 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 MAGNETIC RESONANCE DEVICE ACCESSORY?

The FDA product code for 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.

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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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