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FDA 510(k)

MODEL 460 INTERMITTENT MEDICATION DELIV

K-Number: K823018 · 1983-01-26

ApplicantY
Decision Date1983-01-26
Product CodeFLN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL 460 INTERMITTENT MEDICATION DELIV is the device name listed in this FDA 510(k) record. The listed applicant is Y. It received FDA 510(k) clearance on 1983-01-26 under 510(k) number K823018. 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 MODEL 460 INTERMITTENT MEDICATION DELIV?

MODEL 460 INTERMITTENT MEDICATION DELIV is a medical device that received FDA 510(k) clearance on 1983-01-26. The listed applicant is Y. The 510(k) number is K823018.

When did MODEL 460 INTERMITTENT MEDICATION DELIV receive FDA 510(k) clearance?

MODEL 460 INTERMITTENT MEDICATION DELIV received FDA 510(k) clearance on 1983-01-26, under 510(k) number K823018.

Who is the listed applicant for MODEL 460 INTERMITTENT MEDICATION DELIV?

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

What is the FDA product code for MODEL 460 INTERMITTENT MEDICATION DELIV?

The FDA product code for MODEL 460 INTERMITTENT MEDICATION DELIV is FLN.

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Other records listing Y 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.

K955846MODEL 2082 TEMP PLUS III THERMOMETER/MODEL 2087 TEMP PLUS III WALL MOUNT THERMOMETERK960280IVAC NEEDLE FREE VALVE ADMINISTRATION SETSK953225IVAC BALL VALCE ADMIN. SETSK934095IVAC VENTED SYRINGE ADAPTER ADMINISTRATION SETSK940897IVAC NEEDLELESS INFECTION VALVE ADMINISTRATION SETK931550EZ 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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