FDA 510(k)

MRX-750

K-Number: K933162 · 1993-10-07

Decision Date1993-10-07

Product CodeITY

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MRX-750 is the device name listed in this FDA 510(k) record. The listed applicant is Mrx Corp.. It received FDA 510(k) clearance on 1993-10-07 under 510(k) number K933162. 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-750?

MRX-750 is a medical device that received FDA 510(k) clearance on 1993-10-07. The listed applicant is Mrx Corp.. The 510(k) number is K933162.

When did MRX-750 receive FDA 510(k) clearance?

MRX-750 received FDA 510(k) clearance on 1993-10-07, under 510(k) number K933162.

Who is the listed applicant for MRX-750?

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

What is the FDA product code for MRX-750?

The FDA product code for MRX-750 is ITY.

Other records listing Mrx 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.

K942040MRX-280

Related Devices (Code: ITY)

K000052X-RAY MONOBLOCK, MONOBLOCK XRS-60-330Dynarad Corp.K923094MOLYBDENUMSoutheastern Medical Diagnostics, Inc.K923141PHILIPS PRE-FILTER OPTIONPhilips Medical Systems, Inc.K921129MRX-700Mrx-Ray Tube Corp.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.