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FDA 510(k)

ANGIOGRAPHY CATHETERS

K-Number: K854018 · 1986-01-16

ApplicantMicor, Inc.
Decision Date1986-01-16
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANGIOGRAPHY CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is Micor, Inc.. It received FDA 510(k) clearance on 1986-01-16 under 510(k) number K854018. 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 ANGIOGRAPHY CATHETERS?

ANGIOGRAPHY CATHETERS is a medical device that received FDA 510(k) clearance on 1986-01-16. The listed applicant is Micor, Inc.. The 510(k) number is K854018.

When did ANGIOGRAPHY CATHETERS receive FDA 510(k) clearance?

ANGIOGRAPHY CATHETERS received FDA 510(k) clearance on 1986-01-16, under 510(k) number K854018.

Who is the listed applicant for ANGIOGRAPHY CATHETERS?

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

What is the FDA product code for ANGIOGRAPHY CATHETERS?

The FDA product code for ANGIOGRAPHY CATHETERS is DQO.

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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.

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Other records listing Micor, Inc. as applicant

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.

K031600CONDUCTION CATHETERK003966WUNDCATH CONDUCTION CATHETERK001717MICOR CONDUCTION CATHETERK001940MICOR ANESTHESIA CONDUCTION KITK991879SPRING-WOUND EPIDURAL CATHETERK861008PERCUTANEOUS CATHETERS

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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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