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FDA 510(k)

MAGNETIC RESONANCE DIAGNOSTIC ACCESSORY

K-Number: K953595 · 1995-10-27

ApplicantGE Medical Systems
Decision Date1995-10-27
Product CodeMOS
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 1995-10-27 under 510(k) number K953595. The device is classified under product code MOS. 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 1995-10-27. The listed applicant is GE Medical Systems. The 510(k) number is K953595.

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

MAGNETIC RESONANCE DIAGNOSTIC ACCESSORY received FDA 510(k) clearance on 1995-10-27, under 510(k) number K953595.

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 MOS.

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Other records listing GE Medical Systems as applicant

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Related Devices (Code: MOS)

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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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