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FDA 510(k)

JET PORT PLUS CATHETER SYSTEM

K-Number: K000125 · 2000-04-12

Decision Date2000-04-12
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

JET PORT PLUS CATHETER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Plastic Products SA. It received FDA 510(k) clearance on 2000-04-12 under 510(k) number K000125. 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 JET PORT PLUS CATHETER SYSTEM?

JET PORT PLUS CATHETER SYSTEM is a medical device that received FDA 510(k) clearance on 2000-04-12. The listed applicant is Clinical Plastic Products SA. The 510(k) number is K000125.

When did JET PORT PLUS CATHETER SYSTEM receive FDA 510(k) clearance?

JET PORT PLUS CATHETER SYSTEM received FDA 510(k) clearance on 2000-04-12, under 510(k) number K000125.

Who is the listed applicant for JET PORT PLUS CATHETER SYSTEM?

The FDA 510(k) record lists Clinical Plastic Products SA as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JET PORT PLUS CATHETER SYSTEM?

The FDA product code for JET PORT PLUS 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.

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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