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FDA 510(k)

MATRX MDM, RA

K-Number: K945722 · 1994-12-29

ApplicantMatrx Medical, Inc.
Decision Date1994-12-29
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MATRX MDM, RA is the device name listed in this FDA 510(k) record. The listed applicant is Matrx Medical, Inc.. It received FDA 510(k) clearance on 1994-12-29 under 510(k) number K945722. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATRX MDM, RA?

MATRX MDM, RA is a medical device that received FDA 510(k) clearance on 1994-12-29. The listed applicant is Matrx Medical, Inc.. The 510(k) number is K945722.

When did MATRX MDM, RA receive FDA 510(k) clearance?

MATRX MDM, RA received FDA 510(k) clearance on 1994-12-29, under 510(k) number K945722.

Who is the listed applicant for MATRX MDM, RA?

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

What is the FDA product code for MATRX MDM, RA?

The FDA product code for MATRX MDM, RA is BSZ.

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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.

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