FDA 510(k)

INFUSE-A-PORT HEPARIN LOCK MAINT KIT

K-Number: K840481 · 1984-09-18

Decision Date1984-09-18

Product CodeLJT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

INFUSE-A-PORT HEPARIN LOCK MAINT KIT is the device name listed in this FDA 510(k) record. The listed applicant is Infusaid Corp.. It received FDA 510(k) clearance on 1984-09-18 under 510(k) number K840481. 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 INFUSE-A-PORT HEPARIN LOCK MAINT KIT?

INFUSE-A-PORT HEPARIN LOCK MAINT KIT is a medical device that received FDA 510(k) clearance on 1984-09-18. The listed applicant is Infusaid Corp.. The 510(k) number is K840481.

When did INFUSE-A-PORT HEPARIN LOCK MAINT KIT receive FDA 510(k) clearance?

INFUSE-A-PORT HEPARIN LOCK MAINT KIT received FDA 510(k) clearance on 1984-09-18, under 510(k) number K840481.

Who is the listed applicant for INFUSE-A-PORT HEPARIN LOCK MAINT KIT?

The FDA 510(k) record lists Infusaid Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INFUSE-A-PORT HEPARIN LOCK MAINT KIT?

The FDA product code for INFUSE-A-PORT HEPARIN LOCK MAINT KIT is LJT.

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Other records listing Infusaid Corp. as applicant

K910448SNAP-LOCK MICRO PORT, MODIFICATION K901419DUAL PORT K902251SUBCLAVIAN INTRODUCER SET K860898SUBCLAVIAN INTRODUCER SET K842355INFUSAID INFUSE-A-PORT K832788INFUSE-A-PORT

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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

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