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FDA 510(k)

UMBILICAL VESSEL CATHETER

K-Number: K840339 · 1984-07-25

ApplicantCatheter Technology Corp.
Decision Date1984-07-25
Product CodeFOS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

UMBILICAL VESSEL CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Catheter Technology Corp.. It received FDA 510(k) clearance on 1984-07-25 under 510(k) number K840339. The device is classified under product code FOS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UMBILICAL VESSEL CATHETER?

UMBILICAL VESSEL CATHETER is a medical device that received FDA 510(k) clearance on 1984-07-25. The listed applicant is Catheter Technology Corp.. The 510(k) number is K840339.

When did UMBILICAL VESSEL CATHETER receive FDA 510(k) clearance?

UMBILICAL VESSEL CATHETER received FDA 510(k) clearance on 1984-07-25, under 510(k) number K840339.

Who is the listed applicant for UMBILICAL VESSEL CATHETER?

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

What is the FDA product code for UMBILICAL VESSEL CATHETER?

The FDA product code for UMBILICAL VESSEL CATHETER is FOS.

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Other records listing Catheter Technology 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.

K880571CATH-TECH PORT IMPLANTABLE VASCULAR ACCESS SYSTEMK871080PERIPHERALLY INSERTED CENTRAL VENOUS CATHETERK871998GROSHONG CV CATHETER REPAIR KITK860256BRAWN AND GROSHONG CATHETERSK842577CATH-TECH POLYURETHANE UMBILICAL VESSK842147CATH-TECH CHOLANGIOGRAPHY CATHETER

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Related Devices (Code: FOS)

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.

K201697Umbilical Vessels CatheterHaolang Medical USA CorporationK130725MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR.Covidien Lp, Formerly Registered AS KendallK120304FOOTPRINT MEDICAL POLYURETHANE UMBILICAL CATHETERFootprint Medical, Inc.K091213FOOTPRINT MEDICAL UMBILICAL CATHETER, DUAL LUMENFootprint MedicalK091214FOOTPRINT MEDICAL SILICONE UMBILICAL CATHETERFootprint MedicalK081515NEOMED DUAL LUMEN UMBILICAL CATHETER, MODELS S2UVC4.0, S2UVC5.0Neomed, 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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