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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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