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FDA 510(k)

INFUSE-A-PORT ADDITIONAL SIZES

K-Number: K872329 · 1987-11-13

ApplicantShiley Infusaid, Inc.
Decision Date1987-11-13
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INFUSE-A-PORT ADDITIONAL SIZES is the device name listed in this FDA 510(k) record. The listed applicant is Shiley Infusaid, Inc.. It received FDA 510(k) clearance on 1987-11-13 under 510(k) number K872329. 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 ADDITIONAL SIZES?

INFUSE-A-PORT ADDITIONAL SIZES is a medical device that received FDA 510(k) clearance on 1987-11-13. The listed applicant is Shiley Infusaid, Inc.. The 510(k) number is K872329.

When did INFUSE-A-PORT ADDITIONAL SIZES receive FDA 510(k) clearance?

INFUSE-A-PORT ADDITIONAL SIZES received FDA 510(k) clearance on 1987-11-13, under 510(k) number K872329.

Who is the listed applicant for INFUSE-A-PORT ADDITIONAL SIZES?

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

What is the FDA product code for INFUSE-A-PORT ADDITIONAL SIZES?

The FDA product code for INFUSE-A-PORT ADDITIONAL SIZES 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.

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Other records listing Shiley Infusaid, 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.

K881745INFUSE-A-PORT RADIOPAQUE POLYURETHANE CATHETERK872898POLYURETHANE CATHETER FOR THE INFUSE-A-PORT

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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