The Kendal Co. - FDA 510(k) Cleared Devices
63
Total
60
Cleared
0
Denied
The Kendal Co. has 60 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 60 cleared submissions from 1980 to 2000. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by The Kendal Co. Filter by specialty or product code using the sidebar.
63 devices
Cleared
Mar 17, 2000
MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR
General Hospital
65d
Cleared
Sep 28, 1999
KENDALL ULTRAMER COUDE FOLEY CATHETER, MODEL 1416C, KENDALL CURITY COUDE...
Gastroenterology & Urology
223d
Cleared
Jun 14, 1999
MONOJECT INSULIN SYRINGE
General Hospital
21d
Cleared
Apr 23, 1997
KENDALL CURITY SUPRAPUBIC CATHETER TRAY, KIT, & REPLACEMENT SET
Gastroenterology & Urology
37d
Cleared
Apr 25, 1995
KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAP
Gastroenterology & Urology
25d
Cleared
Jan 17, 1995
KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM
Cardiovascular
225d
Cleared
Jul 20, 1994
POLYSKIN(R) M.R. MOIST RESPONSIVE TRANSPARENT DRESSING
General & Plastic Surgery
37d
Cleared
Aug 15, 1989
KENDALL CURITY OXYGEN MASK
Anesthesiology
127d
Cleared
Jul 24, 1989
KENDALL CURITY INTRAVASCULAR CUT DOWN TUBES
General Hospital
105d
Cleared
Jul 24, 1989
KENDALL CURITY EXTENSION TUBES
General Hospital
105d
Cleared
Jul 14, 1989
KENDALL CURITY IRRIGATION SYRINGE
Gastroenterology & Urology
95d
Cleared
Jun 23, 1989
KENDALL KENGUARD URINARY LEG BAGS
Gastroenterology & Urology
74d
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