FDA 510(k)

TRANSIT INFUSION CATHETER

K-Number: K936260 · 1994-05-31

Decision Date1994-05-31

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

TRANSIT INFUSION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1994-05-31 under 510(k) number K936260. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSIT INFUSION CATHETER?

TRANSIT INFUSION CATHETER is a medical device that received FDA 510(k) clearance on 1994-05-31. The listed applicant is Cordis Corp.. The 510(k) number is K936260.

When did TRANSIT INFUSION CATHETER receive FDA 510(k) clearance?

TRANSIT INFUSION CATHETER received FDA 510(k) clearance on 1994-05-31, under 510(k) number K936260.

Who is the listed applicant for TRANSIT INFUSION CATHETER?

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

What is the FDA product code for TRANSIT INFUSION CATHETER?

The FDA product code for TRANSIT INFUSION CATHETER is DQO.

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Other records listing Cordis Corp. as applicant

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Related Devices (Code: DQO)

K261455Arterial Pressure Monitoring Set/TraySpectrum Vascular K252702Bioptimal Pulmonary Artery Monitoring Catheter (TD2502NF, TD2502NGF, TD2502NDF, TD2502NCF, TD2502NCGF, TD2502NDGF, TD2502NDCF, TD2502NDCGF, TD2502NXCF, TD2502NDXF, TD2502NXCGF, TD2502NDXGF, TD2502NDXCF, TD2502NDXCGF, TD2502-110NF, TD2502-110NGF, TD2502-110NDF, TD2502-110NCF, TD2502-110NDGF, TD2502-110NDCF, TD2502-110NCGF, TD2502-110NDCGF, TD2502-110NXF, TD2502-110NXGF, TD2502-110NDXF, TD2502-110NXCF, TD2502-110NDXGF, TD2502-110NDXCF ,TD2502-110NXCGF, TD2502-110NDXCGF, TD2602NF, TD2602NBioptimal International Pte. , Ltd.K254278Arterial Pressure Monitoring Set/TraySpectrum Vascular K250751DualView CatheterTerumo Corporation K242966Gentuity® HF-OCT Imaging System with Vis-Rx Prime® Micro-Imaging CatheterGentuity, LLC K242420pNOVUS 21 MicrocatheterPhenox, Ltd.

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.