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FDA 510(k)

MPM-NET

K-Number: K030825 · 2003-03-28

Decision Date2003-03-28
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MPM-NET is the device name listed in this FDA 510(k) record. The listed applicant is Aerotel Medical Systems (1998) , Ltd.. It received FDA 510(k) clearance on 2003-03-28 under 510(k) number K030825. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MPM-NET?

MPM-NET is a medical device that received FDA 510(k) clearance on 2003-03-28. The listed applicant is Aerotel Medical Systems (1998) , Ltd.. The 510(k) number is K030825.

When did MPM-NET receive FDA 510(k) clearance?

MPM-NET received FDA 510(k) clearance on 2003-03-28, under 510(k) number K030825.

Who is the listed applicant for MPM-NET?

The FDA 510(k) record lists Aerotel Medical Systems (1998) , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MPM-NET?

The FDA product code for MPM-NET is DXN.

Other records listing Aerotel Medical Systems (1998) , Ltd. as applicant

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.

View all 7 devices →

Related Devices (Code: DXN)

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

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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