FDA 510(k)

MRX-280

K-Number: K942040 · 1994-07-05

Decision Date1994-07-05

Product CodeJAK

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MRX-280 is the device name listed in this FDA 510(k) record. The listed applicant is Mrx Corp.. It received FDA 510(k) clearance on 1994-07-05 under 510(k) number K942040. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MRX-280?

MRX-280 is a medical device that received FDA 510(k) clearance on 1994-07-05. The listed applicant is Mrx Corp.. The 510(k) number is K942040.

When did MRX-280 receive FDA 510(k) clearance?

MRX-280 received FDA 510(k) clearance on 1994-07-05, under 510(k) number K942040.

Who is the listed applicant for MRX-280?

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-280?

The FDA product code for MRX-280 is JAK.

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.

K933162MRX-750

Related Devices (Code: JAK)

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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.