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FDA 510(k)

LEVELERT II FLUID LEVEL SENSOR

K-Number: K060123 · 2006-02-14

ApplicantSmith & Nephew, Inc.
Decision Date2006-02-14
Product CodeFLN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LEVELERT II FLUID LEVEL SENSOR is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2006-02-14 under 510(k) number K060123. 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 LEVELERT II FLUID LEVEL SENSOR?

LEVELERT II FLUID LEVEL SENSOR is a medical device that received FDA 510(k) clearance on 2006-02-14. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K060123.

When did LEVELERT II FLUID LEVEL SENSOR receive FDA 510(k) clearance?

LEVELERT II FLUID LEVEL SENSOR received FDA 510(k) clearance on 2006-02-14, under 510(k) number K060123.

Who is the listed applicant for LEVELERT II FLUID LEVEL SENSOR?

The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LEVELERT II FLUID LEVEL SENSOR?

The FDA product code for LEVELERT II FLUID LEVEL SENSOR is FLN.

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Other records listing Smith & Nephew, Inc. as applicant

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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.K030136DRIP ALERTDrip Alert, Inc.K022248STRYKER L3 HYDROLERTStryker EndoscopyK013121MT ALERT INFUSION MONITORSierra Biosearch, Inc.

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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