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FDA 510(k)

X-PROT DUO PORT

K-Number: K032044 · 2003-07-10

ApplicantC.R. Bard, Inc.
Decision Date2003-07-10
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

X-PROT DUO PORT is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2003-07-10 under 510(k) number K032044. 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 X-PROT DUO PORT?

X-PROT DUO PORT is a medical device that received FDA 510(k) clearance on 2003-07-10. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K032044.

When did X-PROT DUO PORT receive FDA 510(k) clearance?

X-PROT DUO PORT received FDA 510(k) clearance on 2003-07-10, under 510(k) number K032044.

Who is the listed applicant for X-PROT DUO PORT?

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

What is the FDA product code for X-PROT DUO PORT?

The FDA product code for X-PROT DUO PORT is LJT.

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Related Devices (Code: LJT)

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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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