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FDA 510(k)

AC-901 I.V. INFUSION DROP COUNTER

K-Number: K923561 · 1993-05-26

ApplicantLamtic, Inc.
Decision Date1993-05-26
Product CodeFLN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AC-901 I.V. INFUSION DROP COUNTER is the device name listed in this FDA 510(k) record. The listed applicant is Lamtic, Inc.. It received FDA 510(k) clearance on 1993-05-26 under 510(k) number K923561. 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 AC-901 I.V. INFUSION DROP COUNTER?

AC-901 I.V. INFUSION DROP COUNTER is a medical device that received FDA 510(k) clearance on 1993-05-26. The listed applicant is Lamtic, Inc.. The 510(k) number is K923561.

When did AC-901 I.V. INFUSION DROP COUNTER receive FDA 510(k) clearance?

AC-901 I.V. INFUSION DROP COUNTER received FDA 510(k) clearance on 1993-05-26, under 510(k) number K923561.

Who is the listed applicant for AC-901 I.V. INFUSION DROP COUNTER?

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

What is the FDA product code for AC-901 I.V. INFUSION DROP COUNTER?

The FDA product code for AC-901 I.V. INFUSION DROP COUNTER 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.

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Other records listing Lamtic, Inc. 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.

K923560ACCU-DROP I.V. EXTENSION SET

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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