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FDA 510(k) Applications Submitted by THE KENDAL CO.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K970969
03/17/1997
KENDALL CURITY SUPRAPUBIC CATHETER TRAY, KIT, & REPLACEMENT SET
THE KENDAL CO.
K991758
05/24/1999
MONOJECT INSULIN SYRINGE
THE KENDAL CO.
K990500
02/17/1999
KENDALL ULTRAMER COUDE FOLEY CATHETER, MODEL 1416C, KENDALL CURITY COUDE FOLEY CATHETER TRAY, MODEL 6946C
THE KENDAL CO.
K000087
01/12/2000
MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR
THE KENDAL CO.
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