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FDA 510(k)

MATRIX MT-MX3

K-Number: K974700 · 1998-03-04

ApplicantMedtec, Inc.
Decision Date1998-03-04
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MATRIX MT-MX3 is the device name listed in this FDA 510(k) record. The listed applicant is Medtec, Inc.. It received FDA 510(k) clearance on 1998-03-04 under 510(k) number K974700. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATRIX MT-MX3?

MATRIX MT-MX3 is a medical device that received FDA 510(k) clearance on 1998-03-04. The listed applicant is Medtec, Inc.. The 510(k) number is K974700.

When did MATRIX MT-MX3 receive FDA 510(k) clearance?

MATRIX MT-MX3 received FDA 510(k) clearance on 1998-03-04, under 510(k) number K974700.

Who is the listed applicant for MATRIX MT-MX3?

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

What is the FDA product code for MATRIX MT-MX3?

The FDA product code for MATRIX MT-MX3 is IYE.

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Other records listing Medtec, Inc. as applicant

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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