FDA 510(k)

SINGLE, 2&3 WAY SOLUTION SETS #14-070 ET

K-Number: K800618 · 1980-04-24

ApplicantNorton Performance Plastics Corp.

Decision Date1980-04-24

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

SINGLE, 2&3 WAY SOLUTION SETS #14-070 ET is the device name listed in this FDA 510(k) record. The listed applicant is Norton Performance Plastics Corp.. It received FDA 510(k) clearance on 1980-04-24 under 510(k) number K800618. 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 SINGLE, 2&3 WAY SOLUTION SETS #14-070 ET?

SINGLE, 2&3 WAY SOLUTION SETS #14-070 ET is a medical device that received FDA 510(k) clearance on 1980-04-24. The listed applicant is Norton Performance Plastics Corp.. The 510(k) number is K800618.

When did SINGLE, 2&3 WAY SOLUTION SETS #14-070 ET receive FDA 510(k) clearance?

SINGLE, 2&3 WAY SOLUTION SETS #14-070 ET received FDA 510(k) clearance on 1980-04-24, under 510(k) number K800618.

Who is the listed applicant for SINGLE, 2&3 WAY SOLUTION SETS #14-070 ET?

The FDA 510(k) record lists Norton Performance Plastics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SINGLE, 2&3 WAY SOLUTION SETS #14-070 ET?

The FDA product code for SINGLE, 2&3 WAY SOLUTION SETS #14-070 ET is DQO.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Norton Performance Plastics Corp. as applicant

K853791NORTON CARDIOPLEGIC QUICK COOLING COIL 421738-000 K852914ANGIOGRAPHIC, WEDGE PRESS, DUAL THERMOD & INFUSION K851299CORRECT FLO K842858FLUID ADMINISTRATION LINE W/SPIKE 14-923 K841828CENTRAL VENOUS CATHETER W/BIG-GARD K840240MICROFUSE INTRAVENOUS CATHETER SET

View all 39 devices →

Related Devices (Code: DQO)

K261455Arterial Pressure Monitoring Set/TraySpectrum Vascular K252702Bioptimal 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 Vascular K250751DualView CatheterTerumo Corporation K242966Gentuity® HF-OCT Imaging System with Vis-Rx Prime® Micro-Imaging CatheterGentuity, LLC K242420pNOVUS 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.