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FDA 510(k)

MATRIX MICROSON 410

K-Number: K954136 · 1996-04-01

ApplicantMatrix Biokinetics, Inc.
Decision Date1996-04-01
Product CodeIMI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MATRIX MICROSON 410 is the device name listed in this FDA 510(k) record. The listed applicant is Matrix Biokinetics, Inc.. It received FDA 510(k) clearance on 1996-04-01 under 510(k) number K954136. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATRIX MICROSON 410?

MATRIX MICROSON 410 is a medical device that received FDA 510(k) clearance on 1996-04-01. The listed applicant is Matrix Biokinetics, Inc.. The 510(k) number is K954136.

When did MATRIX MICROSON 410 receive FDA 510(k) clearance?

MATRIX MICROSON 410 received FDA 510(k) clearance on 1996-04-01, under 510(k) number K954136.

Who is the listed applicant for MATRIX MICROSON 410?

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

What is the FDA product code for MATRIX MICROSON 410?

The FDA product code for MATRIX MICROSON 410 is IMI.

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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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