PORT-A-CATH DUAL LUMEN IMPLANTABLE VENOUS ACCESS
K-Number: K932841 · 1994-01-05
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Device Summary
Frequently Asked Questions
What is the PORT-A-CATH DUAL LUMEN IMPLANTABLE VENOUS ACCESS?
PORT-A-CATH DUAL LUMEN IMPLANTABLE VENOUS ACCESS is a medical device that received FDA 510(k) clearance on 1994-01-05. The listed applicant is Pharmacia Deltec, Inc.. The 510(k) number is K932841.
When did PORT-A-CATH DUAL LUMEN IMPLANTABLE VENOUS ACCESS receive FDA 510(k) clearance?
PORT-A-CATH DUAL LUMEN IMPLANTABLE VENOUS ACCESS received FDA 510(k) clearance on 1994-01-05, under 510(k) number K932841.
Who is the listed applicant for PORT-A-CATH DUAL LUMEN IMPLANTABLE VENOUS ACCESS?
The FDA 510(k) record lists Pharmacia Deltec, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PORT-A-CATH DUAL LUMEN IMPLANTABLE VENOUS ACCESS?
The FDA product code for PORT-A-CATH DUAL LUMEN IMPLANTABLE VENOUS ACCESS 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 Pharmacia Deltec, 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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