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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