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FDA 510(k)

NORPORT CT-PC, LUCENT NON-CORING NEEDEL INFUSION SET

K-Number: K111101 · 2011-08-25

ApplicantNorfolk Medical
Decision Date2011-08-25
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NORPORT CT-PC, LUCENT NON-CORING NEEDEL INFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Norfolk Medical. It received FDA 510(k) clearance on 2011-08-25 under 510(k) number K111101. 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 NORPORT CT-PC, LUCENT NON-CORING NEEDEL INFUSION SET?

NORPORT CT-PC, LUCENT NON-CORING NEEDEL INFUSION SET is a medical device that received FDA 510(k) clearance on 2011-08-25. The listed applicant is Norfolk Medical. The 510(k) number is K111101.

When did NORPORT CT-PC, LUCENT NON-CORING NEEDEL INFUSION SET receive FDA 510(k) clearance?

NORPORT CT-PC, LUCENT NON-CORING NEEDEL INFUSION SET received FDA 510(k) clearance on 2011-08-25, under 510(k) number K111101.

Who is the listed applicant for NORPORT CT-PC, LUCENT NON-CORING NEEDEL INFUSION SET?

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

What is the FDA product code for NORPORT CT-PC, LUCENT NON-CORING NEEDEL INFUSION SET?

The FDA product code for NORPORT CT-PC, LUCENT NON-CORING NEEDEL INFUSION SET is LJT.

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Other records listing Norfolk Medical 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.

K911067NORCATH VASCULAR ACCESS CATHETERSK905646OMEGAPORT SUBCUTANEOUSLY IMPLANTED DRUG DELIVERY

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

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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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