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FDA 510(k)

LIBERTY SYSTEM

K-Number: K043074 · 2005-02-22

ApplicantInovise Medical, Inc.
Decision Date2005-02-22
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIBERTY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Inovise Medical, Inc.. It received FDA 510(k) clearance on 2005-02-22 under 510(k) number K043074. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIBERTY SYSTEM?

LIBERTY SYSTEM is a medical device that received FDA 510(k) clearance on 2005-02-22. The listed applicant is Inovise Medical, Inc.. The 510(k) number is K043074.

When did LIBERTY SYSTEM receive FDA 510(k) clearance?

LIBERTY SYSTEM received FDA 510(k) clearance on 2005-02-22, under 510(k) number K043074.

Who is the listed applicant for LIBERTY SYSTEM?

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

What is the FDA product code for LIBERTY SYSTEM?

The FDA product code for LIBERTY SYSTEM is DPS.

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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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