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FDA 510(k)

CENTRAL VEIN CATHETERIZATION KIT

K-Number: K800741 · 1980-04-16

ApplicantMedical Components, Inc.
Decision Date1980-04-16
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CENTRAL VEIN CATHETERIZATION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Medical Components, Inc.. It received FDA 510(k) clearance on 1980-04-16 under 510(k) number K800741. 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 CENTRAL VEIN CATHETERIZATION KIT?

CENTRAL VEIN CATHETERIZATION KIT is a medical device that received FDA 510(k) clearance on 1980-04-16. The listed applicant is Medical Components, Inc.. The 510(k) number is K800741.

When did CENTRAL VEIN CATHETERIZATION KIT receive FDA 510(k) clearance?

CENTRAL VEIN CATHETERIZATION KIT received FDA 510(k) clearance on 1980-04-16, under 510(k) number K800741.

Who is the listed applicant for CENTRAL VEIN CATHETERIZATION KIT?

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

What is the FDA product code for CENTRAL VEIN CATHETERIZATION KIT?

The FDA product code for CENTRAL VEIN CATHETERIZATION KIT is DQO.

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Other records listing Medical Components, 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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