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FDA 510(k)

ACCESS QD HEAD COIL

K-Number: K920098 · 1992-06-09

ApplicantToshiba America Mri, Inc.
Decision Date1992-06-09
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ACCESS QD HEAD COIL 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 1992-06-09 under 510(k) number K920098. 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 QD HEAD COIL?

ACCESS QD HEAD COIL is a medical device that received FDA 510(k) clearance on 1992-06-09. The listed applicant is Toshiba America Mri, Inc.. The 510(k) number is K920098.

When did ACCESS QD HEAD COIL receive FDA 510(k) clearance?

ACCESS QD HEAD COIL received FDA 510(k) clearance on 1992-06-09, under 510(k) number K920098.

Who is the listed applicant for ACCESS QD HEAD COIL?

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 QD HEAD COIL?

The FDA product code for ACCESS QD HEAD COIL 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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