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FDA 510(k)

ENTERNAL INFUSER MULTIPUMP 203

K-Number: K861040 · 1986-06-23

ApplicantMedix Medical Electronics (U.S.A.), Inc.
Decision Date1986-06-23
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ENTERNAL INFUSER MULTIPUMP 203 is the device name listed in this FDA 510(k) record. The listed applicant is Medix Medical Electronics (U.S.A.), Inc.. It received FDA 510(k) clearance on 1986-06-23 under 510(k) number K861040. 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 ENTERNAL INFUSER MULTIPUMP 203?

ENTERNAL INFUSER MULTIPUMP 203 is a medical device that received FDA 510(k) clearance on 1986-06-23. The listed applicant is Medix Medical Electronics (U.S.A.), Inc.. The 510(k) number is K861040.

When did ENTERNAL INFUSER MULTIPUMP 203 receive FDA 510(k) clearance?

ENTERNAL INFUSER MULTIPUMP 203 received FDA 510(k) clearance on 1986-06-23, under 510(k) number K861040.

Who is the listed applicant for ENTERNAL INFUSER MULTIPUMP 203?

The FDA 510(k) record lists Medix Medical Electronics (U.S.A.), Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENTERNAL INFUSER MULTIPUMP 203?

The FDA product code for ENTERNAL INFUSER MULTIPUMP 203 is FRN.

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Other records listing Medix Medical Electronics (U.S.A.), 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.

K861001PARENTERAL INFUSER MEDIPUMP 204K853393INSULIN PUMP INSUMAT 229K852433INFUSAFE 205 CATOLOG NO. 205.000K813562SYRINGE DRIVER 209K812039SPIROMETER 210/211K812041VENTI-MONITOR MODEL 101

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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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