JET PORT PLUS HP CATHETER SYSTEM
K-Number: K072481 · 2008-03-07
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Device Summary
Frequently Asked Questions
What is the JET PORT PLUS HP CATHETER SYSTEM?
JET PORT PLUS HP CATHETER SYSTEM is a medical device that received FDA 510(k) clearance on 2008-03-07. The listed applicant is Pfm Medical, Inc.. The 510(k) number is K072481.
When did JET PORT PLUS HP CATHETER SYSTEM receive FDA 510(k) clearance?
JET PORT PLUS HP CATHETER SYSTEM received FDA 510(k) clearance on 2008-03-07, under 510(k) number K072481.
Who is the listed applicant for JET PORT PLUS HP CATHETER SYSTEM?
The FDA 510(k) record lists Pfm Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JET PORT PLUS HP CATHETER SYSTEM?
The FDA product code for JET PORT PLUS HP CATHETER SYSTEM 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 Pfm Medical, 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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