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FDA 510(k)

PORT-A-CATH IMPLANTABLE DRUG DELIVERY SYSTEM

K-Number: K903220 · 1990-10-10

Decision Date1990-10-10
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PORT-A-CATH IMPLANTABLE DRUG DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia Deltec, Inc.. It received FDA 510(k) clearance on 1990-10-10 under 510(k) number K903220. 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 IMPLANTABLE DRUG DELIVERY SYSTEM?

PORT-A-CATH IMPLANTABLE DRUG DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 1990-10-10. The listed applicant is Pharmacia Deltec, Inc.. The 510(k) number is K903220.

When did PORT-A-CATH IMPLANTABLE DRUG DELIVERY SYSTEM receive FDA 510(k) clearance?

PORT-A-CATH IMPLANTABLE DRUG DELIVERY SYSTEM received FDA 510(k) clearance on 1990-10-10, under 510(k) number K903220.

Who is the listed applicant for PORT-A-CATH IMPLANTABLE DRUG DELIVERY SYSTEM?

The FDA 510(k) record lists Pharmacia Deltec, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PORT-A-CATH IMPLANTABLE DRUG DELIVERY SYSTEM?

The FDA product code for PORT-A-CATH IMPLANTABLE DRUG DELIVERY 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 Pharmacia 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 43 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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