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FDA 510(k)

NUMED BALLOON ANGIOGRAPHIC CATHETERS

K-Number: K864940 · 1987-02-19

ApplicantNuMED, Inc.
Decision Date1987-02-19
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NUMED BALLOON ANGIOGRAPHIC CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is NuMED, Inc.. It received FDA 510(k) clearance on 1987-02-19 under 510(k) number K864940. 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 BALLOON ANGIOGRAPHIC CATHETERS?

NUMED BALLOON ANGIOGRAPHIC CATHETERS is a medical device that received FDA 510(k) clearance on 1987-02-19. The listed applicant is NuMED, Inc.. The 510(k) number is K864940.

When did NUMED BALLOON ANGIOGRAPHIC CATHETERS receive FDA 510(k) clearance?

NUMED BALLOON ANGIOGRAPHIC CATHETERS received FDA 510(k) clearance on 1987-02-19, under 510(k) number K864940.

Who is the listed applicant for NUMED BALLOON ANGIOGRAPHIC CATHETERS?

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 BALLOON ANGIOGRAPHIC CATHETERS?

The FDA product code for NUMED BALLOON ANGIOGRAPHIC CATHETERS is DQO.

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Related Devices (Code: DQO)

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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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