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FDA 510(k)

QD WHOLE BODY COIL, MRT-150A

K-Number: K922798 · 1992-09-14

ApplicantToshiba America Mri, Inc.
Decision Date1992-09-14
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

QD WHOLE BODY COIL, MRT-150A 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 1992-09-14 under 510(k) number K922798. 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 QD WHOLE BODY COIL, MRT-150A?

QD WHOLE BODY COIL, MRT-150A is a medical device that received FDA 510(k) clearance on 1992-09-14. The listed applicant is Toshiba America Mri, Inc.. The 510(k) number is K922798.

When did QD WHOLE BODY COIL, MRT-150A receive FDA 510(k) clearance?

QD WHOLE BODY COIL, MRT-150A received FDA 510(k) clearance on 1992-09-14, under 510(k) number K922798.

Who is the listed applicant for QD WHOLE BODY COIL, MRT-150A?

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 QD WHOLE BODY COIL, MRT-150A?

The FDA product code for QD WHOLE BODY COIL, MRT-150A is LNH.

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Other records listing Toshiba America Mri, Inc. as applicant

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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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