FDA 510(k)

PORT-A-CATH(R) IMPLANTABLE DRUG DELIVERY SYSTEM

K-Number: K875276 · 1988-04-13

Decision Date1988-04-13

Product CodeLJT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PORT-A-CATH(R) 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 1988-04-13 under 510(k) number K875276. 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(R) IMPLANTABLE DRUG DELIVERY SYSTEM?

PORT-A-CATH(R) IMPLANTABLE DRUG DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 1988-04-13. The listed applicant is Pharmacia Deltec, Inc.. The 510(k) number is K875276.

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

PORT-A-CATH(R) IMPLANTABLE DRUG DELIVERY SYSTEM received FDA 510(k) clearance on 1988-04-13, under 510(k) number K875276.

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

The FDA product code for PORT-A-CATH(R) 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Pharmacia Deltec, Inc. as applicant

K943310MODEL 6100 AMBULATORY INFUSION SYSTEM K942046PHARMACIA DELTEC EXTENSION SET WITH ANTI-SIPHON VALVE K942161LOCKBOX K942024PORT-A-CATH LOW PROFILE IMPLANTABLE VENOUS ACCESS SYSTEM K941445EXTENSION SET WITH ANTI-SIPHON VALVE K931073CATH-FINDER

View all 43 devices →

Related Devices (Code: LJT)

K260916FLEXI-PORT™ Power Injectable Implantable PortPortal Access, Inc.K252478Vaccess™ CT Low-Profile Power-Injectable Implantable Port; Vaccess™ CT Power-Injectable Implantable Port; PowerPort™ duo M.R.I. ™ Implantable PortBard Access Systems, Inc.K251253PowerPort™ isp Implantable Port; PowerPort™ Slim Implantable Port; PowerPort™ M.R.I. ™ Implantable Port; PowerPort™ M.R.I.™ isp Implantable PortBard Access Systems, Inc.K242328PowerPort™ ClearVUE™ Slim Implantable Ports and PowerPort™ ClearVUE™ Slim Implantable PortsBard Access Systems, Inc.K232737PowerPort™ ClearVUE™ Slim ECG Enabled Implantable Port; PowerPort™ ClearVUE™ isp ECG Enabled Implantable Port; PowerPort™ isp M.R.I.™ ECG Enabled Implantable Port; PowerPort™ Slim ECG Enabled Implantable PortBard Peripheral Vascular, Inc.K190559SmartPort+ Implantable Ports, SmartPort Plastic Implantable PortsAngioDynamics, Inc.

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.