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)

MEDFUSION MODEL 2001 SYRINGE INFUSION PUMP

K-Number: K955231 · 1996-07-18

ApplicantMedex, Inc.
Decision Date1996-07-18
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

MEDFUSION MODEL 2001 SYRINGE INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Medex, Inc.. It received FDA 510(k) clearance on 1996-07-18 under 510(k) number K955231. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the MEDFUSION MODEL 2001 SYRINGE INFUSION PUMP?

MEDFUSION MODEL 2001 SYRINGE INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1996-07-18. The listed applicant is Medex, Inc.. The 510(k) number is K955231.

When did MEDFUSION MODEL 2001 SYRINGE INFUSION PUMP receive FDA 510(k) clearance?

MEDFUSION MODEL 2001 SYRINGE INFUSION PUMP received FDA 510(k) clearance on 1996-07-18, under 510(k) number K955231.

Who is the listed applicant for MEDFUSION MODEL 2001 SYRINGE INFUSION PUMP?

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

What is the FDA product code for MEDFUSION MODEL 2001 SYRINGE INFUSION PUMP?

The FDA product code for MEDFUSION MODEL 2001 SYRINGE INFUSION PUMP is FRN.

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 Medex, Inc. 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.

K042432PHARMGUARD TOOLBOX, MODEL G6000782K040899MEDEX 3000 SERIES MR SYRINGE INFUSION PUMPK020780TRANSTAR INTRACRANIAL PRESSURE TRANSDUCER, MODEL MX950ICPK000328MEDEX 3000 SERIES MRI COMPATIBLE SYRINGE INFUSION PUMPK982640MEDEX 3000 SERIES SYRINGE INFUSION PUMPK982123CONTRAST CONTROL DEVICE

View all 48 devices →

Related Devices (Code: FRN)

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.

K253703RemunityPRO+ Pump for Remodulin® (treprostinil) InjectionDeka R&D CorpK252015FreedomEdge Infusion System; High-Flo SubQ Needle Set; Precision Flow Rate TubingKoru Medical Systems, Inc.K251636Spectrum IQ Infusion System with Dose IQ Safety Software (3570009)Baxter Healthcare CorporationK251640SIGMA Spectrum Infusion Pump with Master Drug LibraryBaxter Healthcare CorporationK242752MRidium 3870 MRI Infusion Pump System (3870)Iradimed CorporationK243855BD Alaris Infusion System with Guardrails Suite MXCarefusion 303, Inc.

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.

↑