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FDA 510(k)

PHARMACIA DELTEC WINGED INFUSION SET

K-Number: K923019 · 1993-04-21

ApplicantPharmacia Deltec, Inc.
Decision Date1993-04-21
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PHARMACIA DELTEC WINGED INFUSION SET 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 1993-04-21 under 510(k) number K923019. 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 PHARMACIA DELTEC WINGED INFUSION SET?

PHARMACIA DELTEC WINGED INFUSION SET is a medical device that received FDA 510(k) clearance on 1993-04-21. The listed applicant is Pharmacia Deltec, Inc.. The 510(k) number is K923019.

When did PHARMACIA DELTEC WINGED INFUSION SET receive FDA 510(k) clearance?

PHARMACIA DELTEC WINGED INFUSION SET received FDA 510(k) clearance on 1993-04-21, under 510(k) number K923019.

Who is the listed applicant for PHARMACIA DELTEC WINGED INFUSION SET?

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 PHARMACIA DELTEC WINGED INFUSION SET?

The FDA product code for PHARMACIA DELTEC WINGED INFUSION SET is LJT.

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Other records listing Pharmacia Deltec, 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.

K943310MODEL 6100 AMBULATORY INFUSION SYSTEMK942046PHARMACIA DELTEC EXTENSION SET WITH ANTI-SIPHON VALVEK942161LOCKBOXK942024PORT-A-CATH LOW PROFILE IMPLANTABLE VENOUS ACCESS SYSTEMK941445EXTENSION SET WITH ANTI-SIPHON VALVEK931073CATH-FINDER

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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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