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FDA 510(k)

CATH-FINDER(TM) CATHETER TRACKING SYSTEM

K-Number: K904150 · 1990-11-19

ApplicantPharmacia Deltec, Inc.
Decision Date1990-11-19
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CATH-FINDER(TM) CATHETER TRACKING SYSTEM 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 1990-11-19 under 510(k) number K904150. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATH-FINDER(TM) CATHETER TRACKING SYSTEM?

CATH-FINDER(TM) CATHETER TRACKING SYSTEM is a medical device that received FDA 510(k) clearance on 1990-11-19. The listed applicant is Pharmacia Deltec, Inc.. The 510(k) number is K904150.

When did CATH-FINDER(TM) CATHETER TRACKING SYSTEM receive FDA 510(k) clearance?

CATH-FINDER(TM) CATHETER TRACKING SYSTEM received FDA 510(k) clearance on 1990-11-19, under 510(k) number K904150.

Who is the listed applicant for CATH-FINDER(TM) CATHETER TRACKING SYSTEM?

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 CATH-FINDER(TM) CATHETER TRACKING SYSTEM?

The FDA product code for CATH-FINDER(TM) CATHETER TRACKING SYSTEM is FOZ.

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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: FOZ)

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.

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum VascularK261041ClearSafe Closed SystemMedSource Labs, LLCK260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLCK253235Introcan Safety® Deep Access XL IV CatheterB.Braun Medical, Inc.K252137BD Insyte™ IV CatheterBecton Dickinson Infusion Therapy Systems, 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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