Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

The Nellcor pulse oximetry monitor interface cable

K-Number: K172482 · 2017-12-15

ApplicantCovidien
Decision Date2017-12-15
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

The Nellcor pulse oximetry monitor interface cable is a medical device manufactured by Covidien. It received FDA 510(k) clearance on 2017-12-15 under approval number K172482. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the The Nellcor pulse oximetry monitor interface cable?

The Nellcor pulse oximetry monitor interface cable is a medical device that received FDA 510(k) clearance on 2017-12-15. It is manufactured by Covidien. The 510(k) number is K172482.

When was The Nellcor pulse oximetry monitor interface cable approved by the FDA?

The Nellcor pulse oximetry monitor interface cable received FDA 510(k) clearance on 2017-12-15, under approval number K172482.

What company makes The Nellcor pulse oximetry monitor interface cable?

The Nellcor pulse oximetry monitor interface cable is manufactured by Covidien.

What is the FDA product code for The Nellcor pulse oximetry monitor interface cable?

The FDA product code for The Nellcor pulse oximetry monitor interface cable is DQA.

Related Clinical Trials

NCT06940752 VINTAGE (Ventricular Intramyocardial Navigation for Tachycardia Ablation Guided by Electrograms) Using Commercial Off-The-Shelf (COTS) Catheters ENROLLING_BY_INVITATION NCT07615738 SpO2 Infant and Pediatric Study NOT_YET_RECRUITING NCT06232876 Continuous Versus Intermittent Ward Monitoring NOT_YET_RECRUITING NCT07608614 Sleep and Performance RECRUITING NCT04121923 Validation of a Novel Device for Screening Patients With Symptoms of Obstructive Sleep Apnea COMPLETED NCT06432881 Investigation of Skin Pigmentation Effect on Performance of Masimo Pulse Oximetry (INSPIRE) RECRUITING

Other Devices by Covidien

K163055Reprocessed Kendall SCD Express Foot Cuff K163102ReliaCatch Specimen Retrieval Bag 10mm; ReliaCatch Specimen Retrieval Bag 12mm K162941Ligasure Blunt Tip, Sealer/Divider, Nano-coated K160718Vital Sync Informatics Manager & Virtual Patient Monitoring Platform K162584VersaOne Bladeless Trocar K161804LigaSure Retractable L-Hook Laparoscopic Sealer/Divider

View all 61 devices →

Related Devices (Code: DQA)

K162675Masimo Rainbow SET Intellivue Module Pulse CO-OximeterMasimo Corporation K160231Model X-100C CO-Met™ Oximetry SystemNonin Medical, Inc. K160940Masimo Disposable Transflectance Forehead SensorMasimo Corporation K153021Fingertip Pulse Oximeter A310Amemo, Inc. K160268Fingertip Pulse Oximeter MD300CG11/MD300CG51Beijing Choice Electronic Technology Co., Ltd. K161560Fingertip Pulse Oximeter MD300CN310Beijing Choice Electronic Technology Co., 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.

↑