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FDA 510(k)

H.U. I.V. DROP COUNTER

K-Number: K893693 · 1989-10-27

ApplicantLi-Lien Corp.
Decision Date1989-10-27
Product CodeFLN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

H.U. I.V. DROP COUNTER is the device name listed in this FDA 510(k) record. The listed applicant is Li-Lien Corp.. It received FDA 510(k) clearance on 1989-10-27 under 510(k) number K893693. 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 H.U. I.V. DROP COUNTER?

H.U. I.V. DROP COUNTER is a medical device that received FDA 510(k) clearance on 1989-10-27. The listed applicant is Li-Lien Corp.. The 510(k) number is K893693.

When did H.U. I.V. DROP COUNTER receive FDA 510(k) clearance?

H.U. I.V. DROP COUNTER received FDA 510(k) clearance on 1989-10-27, under 510(k) number K893693.

Who is the listed applicant for H.U. I.V. DROP COUNTER?

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

What is the FDA product code for H.U. I.V. DROP COUNTER?

The FDA product code for H.U. I.V. DROP COUNTER is FLN.

Related Clinical Trials

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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

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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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