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FDA 510(k)

BARDPORT TITANIUM PORTS

K-Number: K050310 · 2005-04-18

Decision Date2005-04-18
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BARDPORT TITANIUM PORTS is the device name listed in this FDA 510(k) record. The listed applicant is Bard Access Systems, Inc.. It received FDA 510(k) clearance on 2005-04-18 under 510(k) number K050310. 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 BARDPORT TITANIUM PORTS?

BARDPORT TITANIUM PORTS is a medical device that received FDA 510(k) clearance on 2005-04-18. The listed applicant is Bard Access Systems, Inc.. The 510(k) number is K050310.

When did BARDPORT TITANIUM PORTS receive FDA 510(k) clearance?

BARDPORT TITANIUM PORTS received FDA 510(k) clearance on 2005-04-18, under 510(k) number K050310.

Who is the listed applicant for BARDPORT TITANIUM PORTS?

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

What is the FDA product code for BARDPORT TITANIUM PORTS?

The FDA product code for BARDPORT TITANIUM PORTS is LJT.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Bard Access Systems, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 21 devices →

Related Devices (Code: LJT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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