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FDA 510(k)

TWIN-PASS .023 DUAL ACCESS CATHETER, MODEL 5230

K-Number: K062877 · 2007-01-18

ApplicantVascular Solutions, Inc.
Decision Date2007-01-18
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TWIN-PASS .023 DUAL ACCESS CATHETER, MODEL 5230 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 2007-01-18 under 510(k) number K062877. 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 TWIN-PASS .023 DUAL ACCESS CATHETER, MODEL 5230?

TWIN-PASS .023 DUAL ACCESS CATHETER, MODEL 5230 is a medical device that received FDA 510(k) clearance on 2007-01-18. The listed applicant is Vascular Solutions, Inc.. The 510(k) number is K062877.

When did TWIN-PASS .023 DUAL ACCESS CATHETER, MODEL 5230 receive FDA 510(k) clearance?

TWIN-PASS .023 DUAL ACCESS CATHETER, MODEL 5230 received FDA 510(k) clearance on 2007-01-18, under 510(k) number K062877.

Who is the listed applicant for TWIN-PASS .023 DUAL ACCESS CATHETER, MODEL 5230?

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 TWIN-PASS .023 DUAL ACCESS CATHETER, MODEL 5230?

The FDA product code for TWIN-PASS .023 DUAL ACCESS CATHETER, MODEL 5230 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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