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FDA 510(k)

MEDIPORT

K-Number: K060210 · 2006-02-10

ApplicantMaxant Technologies, Inc.
Decision Date2006-02-10
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDIPORT is the device name listed in this FDA 510(k) record. The listed applicant is Maxant Technologies, Inc.. It received FDA 510(k) clearance on 2006-02-10 under 510(k) number K060210. 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 MEDIPORT?

MEDIPORT is a medical device that received FDA 510(k) clearance on 2006-02-10. The listed applicant is Maxant Technologies, Inc.. The 510(k) number is K060210.

When did MEDIPORT receive FDA 510(k) clearance?

MEDIPORT received FDA 510(k) clearance on 2006-02-10, under 510(k) number K060210.

Who is the listed applicant for MEDIPORT?

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

What is the FDA product code for MEDIPORT?

The FDA product code for MEDIPORT is LLZ.

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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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