FDA 510(k) Applications Submitted by PADPRO LLC.

FDA 510(k) Number Submission Date Device Name Applicant
K020203 01/22/2002 PADPRO MODEL #2516 PADPRO LLC.
K020288 01/28/2002 PADPRO, MODEL 2603 PADPRO LLC.
K020743 03/06/2002 PADPRO, MODEL 2502 PADPRO LLC.
K003548 11/17/2000 PADPRO SYSTEM DEFIBRILLATOR ELECTRODE ADAPTERS PADPRO LLC.
K014209 12/21/2001 PADPRO MODEL 2001, 2001-S, 2001-C, 2001-EPS PADPRO LLC.


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