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FDA 510(k)

METRX WORKSTATION

K-Number: K043134 · 2004-12-13

Decision Date2004-12-13
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

METRX WORKSTATION is the device name listed in this FDA 510(k) record. The listed applicant is Medical Metrx Solutions, Inc.. It received FDA 510(k) clearance on 2004-12-13 under 510(k) number K043134. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the METRX WORKSTATION?

METRX WORKSTATION is a medical device that received FDA 510(k) clearance on 2004-12-13. The listed applicant is Medical Metrx Solutions, Inc.. The 510(k) number is K043134.

When did METRX WORKSTATION receive FDA 510(k) clearance?

METRX WORKSTATION received FDA 510(k) clearance on 2004-12-13, under 510(k) number K043134.

Who is the listed applicant for METRX WORKSTATION?

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

What is the FDA product code for METRX WORKSTATION?

The FDA product code for METRX WORKSTATION is LLZ.

Related Clinical Trials

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.

Related Devices (Code: LLZ)

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.

Official Source

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