BD ONECATH
K-Number: K042862 · 2004-12-03
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Device Summary
Frequently Asked Questions
What is the BD ONECATH?
BD ONECATH is a medical device that received FDA 510(k) clearance on 2004-12-03. The listed applicant is Becton Dickinson Infusion Therapy Systems, Inc.. The 510(k) number is K042862.
When did BD ONECATH receive FDA 510(k) clearance?
BD ONECATH received FDA 510(k) clearance on 2004-12-03, under 510(k) number K042862.
Who is the listed applicant for BD ONECATH?
The FDA 510(k) record lists Becton Dickinson Infusion Therapy Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BD ONECATH?
The FDA product code for BD ONECATH is FOZ.
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 Becton Dickinson Infusion Therapy 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: FOZ)
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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