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FDA 510(k)

DROP RATE COUNTER #340

K-Number: K831596 · 1983-07-12

ApplicantImed Corp.
Decision Date1983-07-12
Product CodeFLN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DROP RATE COUNTER #340 is the device name listed in this FDA 510(k) record. The listed applicant is Imed Corp.. It received FDA 510(k) clearance on 1983-07-12 under 510(k) number K831596. 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 RATE COUNTER #340?

DROP RATE COUNTER #340 is a medical device that received FDA 510(k) clearance on 1983-07-12. The listed applicant is Imed Corp.. The 510(k) number is K831596.

When did DROP RATE COUNTER #340 receive FDA 510(k) clearance?

DROP RATE COUNTER #340 received FDA 510(k) clearance on 1983-07-12, under 510(k) number K831596.

Who is the listed applicant for DROP RATE COUNTER #340?

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 RATE COUNTER #340?

The FDA product code for DROP RATE COUNTER #340 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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