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FDA 510(k)

MAMEX

K-Number: K993740 · 1999-11-26

ApplicantMedical Systems Group
Decision Date1999-11-26
Product CodeIZH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAMEX is the device name listed in this FDA 510(k) record. The listed applicant is Medical Systems Group. It received FDA 510(k) clearance on 1999-11-26 under 510(k) number K993740. The device is classified under product code IZH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAMEX?

MAMEX is a medical device that received FDA 510(k) clearance on 1999-11-26. The listed applicant is Medical Systems Group. The 510(k) number is K993740.

When did MAMEX receive FDA 510(k) clearance?

MAMEX received FDA 510(k) clearance on 1999-11-26, under 510(k) number K993740.

Who is the listed applicant for MAMEX?

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

What is the FDA product code for MAMEX?

The FDA product code for MAMEX is IZH.

Related Clinical Trials

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Related Devices (Code: IZH)

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.

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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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