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FDA 510(k)

FLEXART QD BODY COIL

K-Number: K944662 · 1995-01-25

ApplicantToshiba America Mri, Inc.
Decision Date1995-01-25
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FLEXART QD BODY 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 1995-01-25 under 510(k) number K944662. 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 FLEXART QD BODY COIL?

FLEXART QD BODY COIL is a medical device that received FDA 510(k) clearance on 1995-01-25. The listed applicant is Toshiba America Mri, Inc.. The 510(k) number is K944662.

When did FLEXART QD BODY COIL receive FDA 510(k) clearance?

FLEXART QD BODY COIL received FDA 510(k) clearance on 1995-01-25, under 510(k) number K944662.

Who is the listed applicant for FLEXART QD BODY 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 FLEXART QD BODY COIL?

The FDA product code for FLEXART QD BODY COIL 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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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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