510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K030136Substantially Equivalent

Drip Alert

Drip Alert, Inc., Ft. Lauderdale FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K030136 is the FDA 510(k) clearance record for DRIP ALERT, a class II device, cleared for Drip Alert, Inc. on under FDA product code FLN (Monitor, Electric For Gravity Flow Infusion Systems). FDA records list one 510(k) clearance for Drip Alert, Inc. As of , FDA records show no recalls naming K030136.

Clearance record

Decision date
Received
(83 days to decision)
Product code
FLN Monitor, Electric For Gravity Flow Infusion Systems
Regulation
21 CFR 880.2420
Device class
Class II
Review panel
General Hospital
Applicant
Drip Alert, Inc. 500 E. Broward Blvd., Ft. Lauderdale FL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FLN

Trailing 12 months

FDA records hold no clearances under product code FLN in the trailing twelve months.

FDA records show no clearances under product code FLN in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FLN, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260