DRIP ALERT— 510(k) K030136

Substantially Equivalent

Drip Alert, Inc.

FDA 510(k) clearance K030136 for DRIP ALERT, Substantially Equivalent on 2003-04-07. Applicant: Drip Alert, Inc.. Device class: 2.

Clearance details

Applicant: Drip Alert, Inc.
Product code: Code FLN
Device class: Class 2
Regulation: 21 CFR 880.2420
Advisory panel: General Hospital
Date received: 2003-01-14
Decision date: 2003-04-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ft. Lauderdale, FL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.