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FDA 510(k)

MONITOR, GRAVITY IRRIGATION DRIP

K-Number: K781717 · 1978-10-27

ApplicantSyntel, Inc.
Decision Date1978-10-27
Product CodeFLN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MONITOR, GRAVITY IRRIGATION DRIP is the device name listed in this FDA 510(k) record. The listed applicant is Syntel, Inc.. It received FDA 510(k) clearance on 1978-10-27 under 510(k) number K781717. 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 MONITOR, GRAVITY IRRIGATION DRIP?

MONITOR, GRAVITY IRRIGATION DRIP is a medical device that received FDA 510(k) clearance on 1978-10-27. The listed applicant is Syntel, Inc.. The 510(k) number is K781717.

When did MONITOR, GRAVITY IRRIGATION DRIP receive FDA 510(k) clearance?

MONITOR, GRAVITY IRRIGATION DRIP received FDA 510(k) clearance on 1978-10-27, under 510(k) number K781717.

Who is the listed applicant for MONITOR, GRAVITY IRRIGATION DRIP?

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

What is the FDA product code for MONITOR, GRAVITY IRRIGATION DRIP?

The FDA product code for MONITOR, GRAVITY IRRIGATION DRIP 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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