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FDA 510(k)

DUAL PORT

K-Number: K901419 · 1990-09-05

ApplicantInfusaid Corp.
Decision Date1990-09-05
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DUAL PORT is the device name listed in this FDA 510(k) record. The listed applicant is Infusaid Corp.. It received FDA 510(k) clearance on 1990-09-05 under 510(k) number K901419. 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 DUAL PORT?

DUAL PORT is a medical device that received FDA 510(k) clearance on 1990-09-05. The listed applicant is Infusaid Corp.. The 510(k) number is K901419.

When did DUAL PORT receive FDA 510(k) clearance?

DUAL PORT received FDA 510(k) clearance on 1990-09-05, under 510(k) number K901419.

Who is the listed applicant for DUAL PORT?

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 DUAL PORT?

The FDA product code for DUAL PORT is LJT.

Other records listing Infusaid Corp. 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.

K910448SNAP-LOCK MICRO PORT, MODIFICATIONK902251SUBCLAVIAN INTRODUCER SETK860898SUBCLAVIAN INTRODUCER SETK840481INFUSE-A-PORT HEPARIN LOCK MAINT KITK842355INFUSAID INFUSE-A-PORTK832788INFUSE-A-PORT

View all 8 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.

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.

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