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FDA 510(k)

I.V. DRIP MONITOR ALARM DEVICE, MONIFLO

K-Number: K760931 · 1977-01-05

ApplicantDiemolding Corp.
Decision Date1977-01-05
Product CodeFLN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

I.V. DRIP MONITOR ALARM DEVICE, MONIFLO is the device name listed in this FDA 510(k) record. The listed applicant is Diemolding Corp.. It received FDA 510(k) clearance on 1977-01-05 under 510(k) number K760931. 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 I.V. DRIP MONITOR ALARM DEVICE, MONIFLO?

I.V. DRIP MONITOR ALARM DEVICE, MONIFLO is a medical device that received FDA 510(k) clearance on 1977-01-05. The listed applicant is Diemolding Corp.. The 510(k) number is K760931.

When did I.V. DRIP MONITOR ALARM DEVICE, MONIFLO receive FDA 510(k) clearance?

I.V. DRIP MONITOR ALARM DEVICE, MONIFLO received FDA 510(k) clearance on 1977-01-05, under 510(k) number K760931.

Who is the listed applicant for I.V. DRIP MONITOR ALARM DEVICE, MONIFLO?

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

What is the FDA product code for I.V. DRIP MONITOR ALARM DEVICE, MONIFLO?

The FDA product code for I.V. DRIP MONITOR ALARM DEVICE, MONIFLO is FLN.

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Other records listing Diemolding 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.

K962749THERAPEP W/MOUTHPIECE, W/PEDIATRIC MASK, W/SMALL MASK, W/LARGE MASK, RESISTOR/PORT/MOUTHPIECE, RESISTOR/PORTK961455MEDSHIELD/AEROCHAMBERK902713ACCESS. KIT FOR THE BIOSURGE SYNCHRONOUS AUTOTRANSK902114CUFF-MATE 2 ENDOTRACHEAL CUFF INFLATOR & MONITORK900754RESPIREX 2K893791BREATHING MOUTHPIECE

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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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