FDA 510(k)

LIFEPORT VTX ACCESS SYSTEM,MODEL VTX 7000 SERIES

K-Number: K010767 · 2001-04-10

Decision Date2001-04-10

Product CodeLJT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

LIFEPORT VTX ACCESS SYSTEM,MODEL VTX 7000 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Horizon Medical Products, Inc.. It received FDA 510(k) clearance on 2001-04-10 under 510(k) number K010767. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFEPORT VTX ACCESS SYSTEM,MODEL VTX 7000 SERIES?

LIFEPORT VTX ACCESS SYSTEM,MODEL VTX 7000 SERIES is a medical device that received FDA 510(k) clearance on 2001-04-10. The listed applicant is Horizon Medical Products, Inc.. The 510(k) number is K010767.

When did LIFEPORT VTX ACCESS SYSTEM,MODEL VTX 7000 SERIES receive FDA 510(k) clearance?

LIFEPORT VTX ACCESS SYSTEM,MODEL VTX 7000 SERIES received FDA 510(k) clearance on 2001-04-10, under 510(k) number K010767.

Who is the listed applicant for LIFEPORT VTX ACCESS SYSTEM,MODEL VTX 7000 SERIES?

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

What is the FDA product code for LIFEPORT VTX ACCESS SYSTEM,MODEL VTX 7000 SERIES?

The FDA product code for LIFEPORT VTX ACCESS SYSTEM,MODEL VTX 7000 SERIES is LJT.

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Other records listing Horizon Medical Products, Inc. as applicant

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Related Devices (Code: LJT)

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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.