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FDA 510(k)

LIFECLINIC, MODEL 2400

K-Number: K040562 · 2004-08-31

ApplicantLifeclinic International, Inc.
Decision Date2004-08-31
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIFECLINIC, MODEL 2400 is the device name listed in this FDA 510(k) record. The listed applicant is Lifeclinic International, Inc.. It received FDA 510(k) clearance on 2004-08-31 under 510(k) number K040562. 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 LIFECLINIC, MODEL 2400?

LIFECLINIC, MODEL 2400 is a medical device that received FDA 510(k) clearance on 2004-08-31. The listed applicant is Lifeclinic International, Inc.. The 510(k) number is K040562.

When did LIFECLINIC, MODEL 2400 receive FDA 510(k) clearance?

LIFECLINIC, MODEL 2400 received FDA 510(k) clearance on 2004-08-31, under 510(k) number K040562.

Who is the listed applicant for LIFECLINIC, MODEL 2400?

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

What is the FDA product code for LIFECLINIC, MODEL 2400?

The FDA product code for LIFECLINIC, MODEL 2400 is DXN.

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Official Source

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