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FDA 510(k)

LANGSTON DUAL LUMEN PRESSURE MONITORING CATHETER

K-Number: K050168 · 2005-05-18

ApplicantVascular Solutions, Inc.
Decision Date2005-05-18
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LANGSTON DUAL LUMEN PRESSURE MONITORING CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Solutions, Inc.. It received FDA 510(k) clearance on 2005-05-18 under 510(k) number K050168. 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 LANGSTON DUAL LUMEN PRESSURE MONITORING CATHETER?

LANGSTON DUAL LUMEN PRESSURE MONITORING CATHETER is a medical device that received FDA 510(k) clearance on 2005-05-18. The listed applicant is Vascular Solutions, Inc.. The 510(k) number is K050168.

When did LANGSTON DUAL LUMEN PRESSURE MONITORING CATHETER receive FDA 510(k) clearance?

LANGSTON DUAL LUMEN PRESSURE MONITORING CATHETER received FDA 510(k) clearance on 2005-05-18, under 510(k) number K050168.

Who is the listed applicant for LANGSTON DUAL LUMEN PRESSURE MONITORING CATHETER?

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

What is the FDA product code for LANGSTON DUAL LUMEN PRESSURE MONITORING CATHETER?

The FDA product code for LANGSTON DUAL LUMEN PRESSURE MONITORING CATHETER is DQO.

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Related Devices (Code: DQO)

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.

K261455Arterial Pressure Monitoring Set/TraySpectrum VascularK252702Bioptimal 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 VascularK250751DualView CatheterTerumo CorporationK242966Gentuity® HF-OCT Imaging System with Vis-Rx Prime® Micro-Imaging CatheterGentuity, LLCK242420pNOVUS 21 MicrocatheterPhenox, Ltd.

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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