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)

UNIVERSAL DISPOSABLE INFUSION SET (CODE 0330F)

K-Number: K861519 · 1986-05-27

ApplicantJufrey Multimed Corp.
Decision Date1986-05-27
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL DISPOSABLE INFUSION SET (CODE 0330F) is the device name listed in this FDA 510(k) record. The listed applicant is Jufrey Multimed Corp.. It received FDA 510(k) clearance on 1986-05-27 under 510(k) number K861519. 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 UNIVERSAL DISPOSABLE INFUSION SET (CODE 0330F)?

UNIVERSAL DISPOSABLE INFUSION SET (CODE 0330F) is a medical device that received FDA 510(k) clearance on 1986-05-27. The listed applicant is Jufrey Multimed Corp.. The 510(k) number is K861519.

When did UNIVERSAL DISPOSABLE INFUSION SET (CODE 0330F) receive FDA 510(k) clearance?

UNIVERSAL DISPOSABLE INFUSION SET (CODE 0330F) received FDA 510(k) clearance on 1986-05-27, under 510(k) number K861519.

Who is the listed applicant for UNIVERSAL DISPOSABLE INFUSION SET (CODE 0330F)?

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

What is the FDA product code for UNIVERSAL DISPOSABLE INFUSION SET (CODE 0330F)?

The FDA product code for UNIVERSAL DISPOSABLE INFUSION SET (CODE 0330F) 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 Jufrey Multimed Corp. 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.

K861518UNIVERSAL DISPOSABLE INFUSION SET (CODE 0205F)K861520UNIVERSAL DISPOSABLE INFUSION SET (CODE 0205)K861523STANDARD BLOOD TRANSFUSION FILTER SET (CODE 1025)K861521UNIVERSAL DISPOSABLE INFUSION SET (CODE 0330)K853527JUFREY CORP. UNIV. DISPOS. SCALP VEIN INFUSION SETK853327JUFREY CORP. UNIVERSAL DISPOS. SCALP VEIN INFUSION

View all 7 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.

↑