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)

LUTHER SAFETY HUBER NEEDLE SET

K-Number: K021565 · 2002-11-14

ApplicantLuther Research Partners
Decision Date2002-11-14
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LUTHER SAFETY HUBER NEEDLE SET is the device name listed in this FDA 510(k) record. The listed applicant is Luther Research Partners. It received FDA 510(k) clearance on 2002-11-14 under 510(k) number K021565. 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 LUTHER SAFETY HUBER NEEDLE SET?

LUTHER SAFETY HUBER NEEDLE SET is a medical device that received FDA 510(k) clearance on 2002-11-14. The listed applicant is Luther Research Partners. The 510(k) number is K021565.

When did LUTHER SAFETY HUBER NEEDLE SET receive FDA 510(k) clearance?

LUTHER SAFETY HUBER NEEDLE SET received FDA 510(k) clearance on 2002-11-14, under 510(k) number K021565.

Who is the listed applicant for LUTHER SAFETY HUBER NEEDLE SET?

The FDA 510(k) record lists Luther Research Partners as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LUTHER SAFETY HUBER NEEDLE SET?

The FDA product code for LUTHER SAFETY HUBER NEEDLE SET 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

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.

↑