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FDA 510(k)

DROP CONTROLLER

K-Number: K790669 · 1979-05-14

ApplicantImed Corp.
Decision Date1979-05-14
Product CodeFLN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DROP CONTROLLER is the device name listed in this FDA 510(k) record. The listed applicant is Imed Corp.. It received FDA 510(k) clearance on 1979-05-14 under 510(k) number K790669. The device is classified under product code FLN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DROP CONTROLLER?

DROP CONTROLLER is a medical device that received FDA 510(k) clearance on 1979-05-14. The listed applicant is Imed Corp.. The 510(k) number is K790669.

When did DROP CONTROLLER receive FDA 510(k) clearance?

DROP CONTROLLER received FDA 510(k) clearance on 1979-05-14, under 510(k) number K790669.

Who is the listed applicant for DROP CONTROLLER?

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 DROP CONTROLLER?

The FDA product code for DROP CONTROLLER is FLN.

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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: FLN)

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.

K172242DripAssist PlusShift Labs, Inc.K080704LOW FLUID ALARMEm-Tec GmbHK050783ISSYS DRUG FLOW MONITORIntegrated Sensing Systems, Inc.K060123LEVELERT II FLUID LEVEL SENSORSmith & Nephew, Inc.K030136DRIP ALERTDrip Alert, Inc.K022248STRYKER L3 HYDROLERTStryker Endoscopy

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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