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)

AUTOFUSER AMBULATORY INFUSION PUMP

K-Number: K041585 · 2004-08-26

ApplicantAlgos, LC
Decision Date2004-08-26
Product CodeMEB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AUTOFUSER AMBULATORY INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Algos, LC. It received FDA 510(k) clearance on 2004-08-26 under 510(k) number K041585. The device is classified under product code MEB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOFUSER AMBULATORY INFUSION PUMP?

AUTOFUSER AMBULATORY INFUSION PUMP is a medical device that received FDA 510(k) clearance on 2004-08-26. The listed applicant is Algos, LC. The 510(k) number is K041585.

When did AUTOFUSER AMBULATORY INFUSION PUMP receive FDA 510(k) clearance?

AUTOFUSER AMBULATORY INFUSION PUMP received FDA 510(k) clearance on 2004-08-26, under 510(k) number K041585.

Who is the listed applicant for AUTOFUSER AMBULATORY INFUSION PUMP?

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

What is the FDA product code for AUTOFUSER AMBULATORY INFUSION PUMP?

The FDA product code for AUTOFUSER AMBULATORY INFUSION PUMP is MEB.

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: MEB)

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.

K250234SMARTeZ™ Elastomeric Infusion Pump (RS series)Epic Medical Pte. , Ltd.K240624InfuLifeFirst Medical Source, LLCK242152SMARTeZ™ Elastomeric Infusion Pump (498111, 498121, 498131, 498141)Epic Medical Pte. , Ltd.K181360ON-Q* Pump with BolusHalyard HealthK151650SMARTez elastomeric infusion pumpEpic Medical Pte. , Ltd.K131247MULTIBOLUS II DISPOSABLE PAIN MANAGEMENT SYSTEMMfs - Medical Flow Systems, Ltd.

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.

↑