BARDPORT TITANIUM PORTS
K-Number: K050310 · 2005-04-18
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Device Summary
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.
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
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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