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FDA 510(k)

NUMED ATRIOSEPTOSTOMY CATHETER

K-Number: K960070 · 1996-04-02

ApplicantNuMED, Inc.
Decision Date1996-04-02
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NUMED ATRIOSEPTOSTOMY CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is NuMED, Inc.. It received FDA 510(k) clearance on 1996-04-02 under 510(k) number K960070. 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 NUMED ATRIOSEPTOSTOMY CATHETER?

NUMED ATRIOSEPTOSTOMY CATHETER is a medical device that received FDA 510(k) clearance on 1996-04-02. The listed applicant is NuMED, Inc.. The 510(k) number is K960070.

When did NUMED ATRIOSEPTOSTOMY CATHETER receive FDA 510(k) clearance?

NUMED ATRIOSEPTOSTOMY CATHETER received FDA 510(k) clearance on 1996-04-02, under 510(k) number K960070.

Who is the listed applicant for NUMED ATRIOSEPTOSTOMY CATHETER?

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

What is the FDA product code for NUMED ATRIOSEPTOSTOMY CATHETER?

The FDA product code for NUMED ATRIOSEPTOSTOMY 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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