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

FDA 510(k)

NEXUS INJECTION SITE (NIS), MODEL NIS-1

K-Number: K024363 · 2003-02-19

ApplicantNexus Medical, LLC
Decision Date2003-02-19
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NEXUS INJECTION SITE (NIS), MODEL NIS-1 is the device name listed in this FDA 510(k) record. The listed applicant is Nexus Medical, LLC. It received FDA 510(k) clearance on 2003-02-19 under 510(k) number K024363. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEXUS INJECTION SITE (NIS), MODEL NIS-1?

NEXUS INJECTION SITE (NIS), MODEL NIS-1 is a medical device that received FDA 510(k) clearance on 2003-02-19. The listed applicant is Nexus Medical, LLC. The 510(k) number is K024363.

When did NEXUS INJECTION SITE (NIS), MODEL NIS-1 receive FDA 510(k) clearance?

NEXUS INJECTION SITE (NIS), MODEL NIS-1 received FDA 510(k) clearance on 2003-02-19, under 510(k) number K024363.

Who is the listed applicant for NEXUS INJECTION SITE (NIS), MODEL NIS-1?

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

What is the FDA product code for NEXUS INJECTION SITE (NIS), MODEL NIS-1?

The FDA product code for NEXUS INJECTION SITE (NIS), MODEL NIS-1 is FPA.

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_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Nexus Medical, LLC 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.

K130879NEXUS IV TUBING SET WITH LUER-ACCESSBILE ONE-WAY CHECK VALVE - IV PLUSK130416NEXUS TKO-6P LUER ACTIVATED DEVICEK113398NEXUS TKO-6, LUER-ACTIVATED DEVICEK092382NEXUS PRESSURE RATED EXTENSION SETSK092930NEXUS INTRAVASCULAR TUBING SETS-PRE-PIERCEDK092527NEXUS INJECTION SITE, MODEL NIS-8

View all 14 devices →

Related Devices (Code: FPA)

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.

K254123Ecomed Disposable Administration SetsEcomed Solutions, LLCK261530iiSure Infusion SetDeka Research and DevelopmentK252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)Amsino International, Inc.K251375PuraCath Firefly Needleless Connector IT (9005)Puracath Medical, Inc.K251257nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free Connector (NFC) [6426731]; nSyte Needle Free Connector (NFC) [6426727]Np MedicalK250325BD Alaris Pump Infusion SetCarefusion (Bd)

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.

↑