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FDA 510(k)

KHM 2000 DRIP WATCHER

K-Number: K844556 · 1985-01-14

ApplicantThe Timeter Group
Decision Date1985-01-14
Product CodeFLN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

KHM 2000 DRIP WATCHER is the device name listed in this FDA 510(k) record. The listed applicant is The Timeter Group. It received FDA 510(k) clearance on 1985-01-14 under 510(k) number K844556. 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 KHM 2000 DRIP WATCHER?

KHM 2000 DRIP WATCHER is a medical device that received FDA 510(k) clearance on 1985-01-14. The listed applicant is The Timeter Group. The 510(k) number is K844556.

When did KHM 2000 DRIP WATCHER receive FDA 510(k) clearance?

KHM 2000 DRIP WATCHER received FDA 510(k) clearance on 1985-01-14, under 510(k) number K844556.

Who is the listed applicant for KHM 2000 DRIP WATCHER?

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

What is the FDA product code for KHM 2000 DRIP WATCHER?

The FDA product code for KHM 2000 DRIP WATCHER is FLN.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing The Timeter Group 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.

K871452CLASSIC (TM) 200 OXYGEN FLOWMETERK862171MP-500 ELECTRONIC NEBULIZERK852374OXYGEN REGULATORS #50 PRT & BGT(BGT15,BGT18

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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