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FDA 510(k)

SNR-3000 UPGRADE RECEIVER COILS

K-Number: K925597 · 1993-10-07

ApplicantMagnetic Resonance Plus, Inc.
Decision Date1993-10-07
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SNR-3000 UPGRADE RECEIVER COILS is the device name listed in this FDA 510(k) record. The listed applicant is Magnetic Resonance Plus, Inc.. It received FDA 510(k) clearance on 1993-10-07 under 510(k) number K925597. 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 SNR-3000 UPGRADE RECEIVER COILS?

SNR-3000 UPGRADE RECEIVER COILS is a medical device that received FDA 510(k) clearance on 1993-10-07. The listed applicant is Magnetic Resonance Plus, Inc.. The 510(k) number is K925597.

When did SNR-3000 UPGRADE RECEIVER COILS receive FDA 510(k) clearance?

SNR-3000 UPGRADE RECEIVER COILS received FDA 510(k) clearance on 1993-10-07, under 510(k) number K925597.

Who is the listed applicant for SNR-3000 UPGRADE RECEIVER COILS?

The FDA 510(k) record lists Magnetic Resonance Plus, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SNR-3000 UPGRADE RECEIVER COILS?

The FDA product code for SNR-3000 UPGRADE RECEIVER COILS is LNH.

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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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