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FDA 510(k)

AUTOMED 3200 INFUSION PUMP

K-Number: K023973 · 2003-02-27

ApplicantHelp Technologies
Decision Date2003-02-27
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AUTOMED 3200 INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Help Technologies. It received FDA 510(k) clearance on 2003-02-27 under 510(k) number K023973. 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 AUTOMED 3200 INFUSION PUMP?

AUTOMED 3200 INFUSION PUMP is a medical device that received FDA 510(k) clearance on 2003-02-27. The listed applicant is Help Technologies. The 510(k) number is K023973.

When did AUTOMED 3200 INFUSION PUMP receive FDA 510(k) clearance?

AUTOMED 3200 INFUSION PUMP received FDA 510(k) clearance on 2003-02-27, under 510(k) number K023973.

Who is the listed applicant for AUTOMED 3200 INFUSION PUMP?

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

What is the FDA product code for AUTOMED 3200 INFUSION PUMP?

The FDA product code for AUTOMED 3200 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 Help Technologies 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.

K023863AUTOMED 3000 INFUSION PUMPK023491AUTOMED 3300 AND 3400 INFUSION PUMP SYSTEMK003915ACCUFUSER; ACCUFUSER PLUS

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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