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FDA 510(k)

MAGNETIC RESONANCE DIAGNOSTIC ACCESSORY

K-Number: K934499 · 1993-12-23

ApplicantGE Medical Systems
Decision Date1993-12-23
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAGNETIC RESONANCE DIAGNOSTIC ACCESSORY is the device name listed in this FDA 510(k) record. The listed applicant is GE Medical Systems. It received FDA 510(k) clearance on 1993-12-23 under 510(k) number K934499. 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 MAGNETIC RESONANCE DIAGNOSTIC ACCESSORY?

MAGNETIC RESONANCE DIAGNOSTIC ACCESSORY is a medical device that received FDA 510(k) clearance on 1993-12-23. The listed applicant is GE Medical Systems. The 510(k) number is K934499.

When did MAGNETIC RESONANCE DIAGNOSTIC ACCESSORY receive FDA 510(k) clearance?

MAGNETIC RESONANCE DIAGNOSTIC ACCESSORY received FDA 510(k) clearance on 1993-12-23, under 510(k) number K934499.

Who is the listed applicant for MAGNETIC RESONANCE DIAGNOSTIC ACCESSORY?

The FDA 510(k) record lists GE Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAGNETIC RESONANCE DIAGNOSTIC ACCESSORY?

The FDA product code for MAGNETIC RESONANCE DIAGNOSTIC ACCESSORY is LNH.

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Other records listing GE Medical Systems 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.

K253808AIR Recon DLK220848Venue FitK220851VenueK173341Vivid E80, Vivid E90, Vivid E95K103411IDEAL IQ SOFTWARE OPTIONK073138CARDIQ EXPRESS VERSION 2.0

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Related Devices (Code: LNH)

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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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