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FDA 510(k)

MODEL 3001 SYRINGE INFUSION PUMP

K-Number: K901755 · 1990-08-29

ApplicantMedfusion, Inc.
Decision Date1990-08-29
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL 3001 SYRINGE INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Medfusion, Inc.. It received FDA 510(k) clearance on 1990-08-29 under 510(k) number K901755. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 3001 SYRINGE INFUSION PUMP?

MODEL 3001 SYRINGE INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1990-08-29. The listed applicant is Medfusion, Inc.. The 510(k) number is K901755.

When did MODEL 3001 SYRINGE INFUSION PUMP receive FDA 510(k) clearance?

MODEL 3001 SYRINGE INFUSION PUMP received FDA 510(k) clearance on 1990-08-29, under 510(k) number K901755.

Who is the listed applicant for MODEL 3001 SYRINGE INFUSION PUMP?

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

What is the FDA product code for MODEL 3001 SYRINGE INFUSION PUMP?

The FDA product code for MODEL 3001 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 Medfusion, 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.

K905783MODIFIED WALKMED 400K905029MODEL 2001, MODIFICATIONK890862AMBULATORY INFUSION PUMPK890120SYRINGE INFUSION PUMP

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.

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