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FDA 510(k)

C-PORT - HP POWER INJECTABLE PORT

K-Number: K091099 · 2009-05-22

Decision Date2009-05-22
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

C-PORT - HP POWER INJECTABLE PORT is the device name listed in this FDA 510(k) record. The listed applicant is Phs Medical GmbH. It received FDA 510(k) clearance on 2009-05-22 under 510(k) number K091099. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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