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FDA 510(k)

GUIDING CATHETERS 9F JL4

K-Number: K871021 · 1987-06-16

ApplicantDevices For Vascular Intervention, Inc.
Decision Date1987-06-16
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

GUIDING CATHETERS 9F JL4 is the device name listed in this FDA 510(k) record. The listed applicant is Devices For Vascular Intervention, Inc.. It received FDA 510(k) clearance on 1987-06-16 under 510(k) number K871021. 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 GUIDING CATHETERS 9F JL4?

GUIDING CATHETERS 9F JL4 is a medical device that received FDA 510(k) clearance on 1987-06-16. The listed applicant is Devices For Vascular Intervention, Inc.. The 510(k) number is K871021.

When did GUIDING CATHETERS 9F JL4 receive FDA 510(k) clearance?

GUIDING CATHETERS 9F JL4 received FDA 510(k) clearance on 1987-06-16, under 510(k) number K871021.

Who is the listed applicant for GUIDING CATHETERS 9F JL4?

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

What is the FDA product code for GUIDING CATHETERS 9F JL4?

The FDA product code for GUIDING CATHETERS 9F JL4 is DQO.

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Other records listing Devices For Vascular Intervention, Inc. as applicant

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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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