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FDA 510(k)

IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICE

K-Number: K895797 · 1990-01-02

ApplicantImed Corp.
Decision Date1990-01-02
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Imed Corp.. It received FDA 510(k) clearance on 1990-01-02 under 510(k) number K895797. 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 IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICE?

IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICE is a medical device that received FDA 510(k) clearance on 1990-01-02. The listed applicant is Imed Corp.. The 510(k) number is K895797.

When did IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICE receive FDA 510(k) clearance?

IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICE received FDA 510(k) clearance on 1990-01-02, under 510(k) number K895797.

Who is the listed applicant for IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICE?

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

What is the FDA product code for IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICE?

The FDA product code for IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICE is FRN.

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Other records listing Imed 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.

K960512GEMINI PC-ITXK953896THE IMED AMBULATORY INFUSION PUMP, ADMINISTRATION SETSK950153VENTED/NONVENTED GEMINI ADMINISTRATION SET WITH CHECK VALVE AND TWO SAFSITE(TM) VALVESK951922ADMINISTRATION SETS WITH BALL FLOATK950419THE IMED ORION INFUSION PUMP AND ADMINISTRATION SETSK944320VENTED/NON-VENTED GEMINI ADMINISTRATION SET

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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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