FDA 510(k)

MRX-700

K-Number: K921129 · 1992-10-05

Decision Date1992-10-05

Product CodeITY

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MRX-700 is the device name listed in this FDA 510(k) record. The listed applicant is Mrx-Ray Tube Corp.. It received FDA 510(k) clearance on 1992-10-05 under 510(k) number K921129. The device is classified under product code ITY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MRX-700?

MRX-700 is a medical device that received FDA 510(k) clearance on 1992-10-05. The listed applicant is Mrx-Ray Tube Corp.. The 510(k) number is K921129.

When did MRX-700 receive FDA 510(k) clearance?

MRX-700 received FDA 510(k) clearance on 1992-10-05, under 510(k) number K921129.

Who is the listed applicant for MRX-700?

The FDA 510(k) record lists Mrx-Ray Tube Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MRX-700?

The FDA product code for MRX-700 is ITY.

Other records listing Mrx-Ray Tube Corp. 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.

K921130MRX-865

Related Devices (Code: ITY)

K000052X-RAY MONOBLOCK, MONOBLOCK XRS-60-330Dynarad Corp.K933162MRX-750Mrx Corp.K923094MOLYBDENUMSoutheastern Medical Diagnostics, Inc.K923141PHILIPS PRE-FILTER OPTIONPhilips Medical Systems, Inc.K921130MRX-865Mrx-Ray Tube Corp.K921316MG-1001 TUBE HOUSING ASSEMBLYMagma Corp.

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.