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FDA 510(k)

TRILOGY INFUSION PUMP

K-Number: K925311 · 1993-08-16

ApplicantIvion Corp.
Decision Date1993-08-16
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TRILOGY INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Ivion Corp.. It received FDA 510(k) clearance on 1993-08-16 under 510(k) number K925311. 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 TRILOGY INFUSION PUMP?

TRILOGY INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1993-08-16. The listed applicant is Ivion Corp.. The 510(k) number is K925311.

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

TRILOGY INFUSION PUMP received FDA 510(k) clearance on 1993-08-16, under 510(k) number K925311.

Who is the listed applicant for TRILOGY INFUSION PUMP?

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

What is the FDA product code for TRILOGY INFUSION PUMP?

The FDA product code for TRILOGY 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.

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Other records listing Ivion Corp. 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.

K925219IVION ADMIN SETS W/FLOW CLIPSK920036SURECATH PORT ACCESS CATHETER

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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