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FDA 510(k)

DRIP ALERT

K-Number: K030136 · 2003-04-07

Decision Date2003-04-07
Product CodeFLN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DRIP ALERT is the device name listed in this FDA 510(k) record. The listed applicant is Drip Alert, Inc.. It received FDA 510(k) clearance on 2003-04-07 under 510(k) number K030136. 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 DRIP ALERT?

DRIP ALERT is a medical device that received FDA 510(k) clearance on 2003-04-07. The listed applicant is Drip Alert, Inc.. The 510(k) number is K030136.

When did DRIP ALERT receive FDA 510(k) clearance?

DRIP ALERT received FDA 510(k) clearance on 2003-04-07, under 510(k) number K030136.

Who is the listed applicant for DRIP ALERT?

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

What is the FDA product code for DRIP ALERT?

The FDA product code for DRIP ALERT 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.

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.

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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