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FDA 510(k)

MRI RESONANCE DIAGNOSTIC DEVICE ACCESORY

K-Number: K934538 · 1994-04-25

ApplicantNoise Cancellation Technologies
Decision Date1994-04-25
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MRI RESONANCE DIAGNOSTIC DEVICE ACCESORY is the device name listed in this FDA 510(k) record. The listed applicant is Noise Cancellation Technologies. It received FDA 510(k) clearance on 1994-04-25 under 510(k) number K934538. 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 MRI RESONANCE DIAGNOSTIC DEVICE ACCESORY?

MRI RESONANCE DIAGNOSTIC DEVICE ACCESORY is a medical device that received FDA 510(k) clearance on 1994-04-25. The listed applicant is Noise Cancellation Technologies. The 510(k) number is K934538.

When did MRI RESONANCE DIAGNOSTIC DEVICE ACCESORY receive FDA 510(k) clearance?

MRI RESONANCE DIAGNOSTIC DEVICE ACCESORY received FDA 510(k) clearance on 1994-04-25, under 510(k) number K934538.

Who is the listed applicant for MRI RESONANCE DIAGNOSTIC DEVICE ACCESORY?

The FDA 510(k) record lists Noise Cancellation Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MRI RESONANCE DIAGNOSTIC DEVICE ACCESORY?

The FDA product code for MRI RESONANCE DIAGNOSTIC DEVICE ACCESORY is LNH.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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