DRIP ALERT


Device Classification Name

monitor, electric for gravity flow infusion systems

510(k) Number K030136
Device Name DRIP ALERT
Original Applicant
DRIP ALERT, INC.
500 e. broward blvd.
suite 1400
ft. lauderdale, 
FL 
33394

Original Contact polly d heseman
Regulation Number 880.2420
Classification Product Code
FLN  
Date Received 01/14/2003
Decision Date 04/07/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General Hospital

510k Review Panel

General Hospital

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No