C-PORT - HP POWER INJECTABLE PORT
K-Number: K091099 · 2009-05-22
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Device Summary
Frequently Asked Questions
What is the C-PORT - HP POWER INJECTABLE PORT?
C-PORT - HP POWER INJECTABLE PORT is a medical device that received FDA 510(k) clearance on 2009-05-22. The listed applicant is Phs Medical GmbH. The 510(k) number is K091099.
When did C-PORT - HP POWER INJECTABLE PORT receive FDA 510(k) clearance?
C-PORT - HP POWER INJECTABLE PORT received FDA 510(k) clearance on 2009-05-22, under 510(k) number K091099.
Who is the listed applicant for C-PORT - HP POWER INJECTABLE PORT?
The FDA 510(k) record lists Phs Medical GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for C-PORT - HP POWER INJECTABLE PORT?
The FDA product code for C-PORT - HP POWER INJECTABLE PORT 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.
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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