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FDA 510(k)

PORT-A-CATH DUAL LUMEN IMPLANTABLE VENOUS

K-Number: K955407 · 1996-02-12

Decision Date1996-02-12
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PORT-A-CATH DUAL LUMEN IMPLANTABLE VENOUS is the device name listed in this FDA 510(k) record. The listed applicant is Sims Deltec, Inc.. It received FDA 510(k) clearance on 1996-02-12 under 510(k) number K955407. 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 PORT-A-CATH DUAL LUMEN IMPLANTABLE VENOUS?

PORT-A-CATH DUAL LUMEN IMPLANTABLE VENOUS is a medical device that received FDA 510(k) clearance on 1996-02-12. The listed applicant is Sims Deltec, Inc.. The 510(k) number is K955407.

When did PORT-A-CATH DUAL LUMEN IMPLANTABLE VENOUS receive FDA 510(k) clearance?

PORT-A-CATH DUAL LUMEN IMPLANTABLE VENOUS received FDA 510(k) clearance on 1996-02-12, under 510(k) number K955407.

Who is the listed applicant for PORT-A-CATH DUAL LUMEN IMPLANTABLE VENOUS?

The FDA 510(k) record lists Sims 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?

The FDA product code for PORT-A-CATH DUAL LUMEN IMPLANTABLE VENOUS 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 Sims 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.

View all 32 devices →

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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