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FDA 510(k)

MAP MULTITRACK ANGIOGRAPHIC CATHETER (4F)

K-Number: K952984 · 1996-01-29

ApplicantMap Medical Equipment, Inc.
Decision Date1996-01-29
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MAP MULTITRACK ANGIOGRAPHIC CATHETER (4F) is the device name listed in this FDA 510(k) record. The listed applicant is Map Medical Equipment, Inc.. It received FDA 510(k) clearance on 1996-01-29 under 510(k) number K952984. 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 MAP MULTITRACK ANGIOGRAPHIC CATHETER (4F)?

MAP MULTITRACK ANGIOGRAPHIC CATHETER (4F) is a medical device that received FDA 510(k) clearance on 1996-01-29. The listed applicant is Map Medical Equipment, Inc.. The 510(k) number is K952984.

When did MAP MULTITRACK ANGIOGRAPHIC CATHETER (4F) receive FDA 510(k) clearance?

MAP MULTITRACK ANGIOGRAPHIC CATHETER (4F) received FDA 510(k) clearance on 1996-01-29, under 510(k) number K952984.

Who is the listed applicant for MAP MULTITRACK ANGIOGRAPHIC CATHETER (4F)?

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

What is the FDA product code for MAP MULTITRACK ANGIOGRAPHIC CATHETER (4F)?

The FDA product code for MAP MULTITRACK ANGIOGRAPHIC CATHETER (4F) 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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