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FDA 510(k)

IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICES MOD

K-Number: K913658 · 1992-03-26

ApplicantImed Corp.
Decision Date1992-03-26
Product CodeMEB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICES MOD is the device name listed in this FDA 510(k) record. The listed applicant is Imed Corp.. It received FDA 510(k) clearance on 1992-03-26 under 510(k) number K913658. 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 IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICES MOD?

IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICES MOD is a medical device that received FDA 510(k) clearance on 1992-03-26. The listed applicant is Imed Corp.. The 510(k) number is K913658.

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

IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICES MOD received FDA 510(k) clearance on 1992-03-26, under 510(k) number K913658.

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

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 DEVICES MOD?

The FDA product code for IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICES MOD is MEB.

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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: 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.

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