Kendall Healthcare Products Co. Div.Of Tyco Health - FDA 510(k) Clear...
66
Total
50
Cleared
0
Denied
Kendall Healthcare Products Co. Div.Of Tyco Health has 50 FDA 510(k) cleared medical devices. Based in Mansfield, US.
Historical record: 50 cleared submissions from 1989 to 1997.
Browse the FDA 510(k) cleared devices submitted by Kendall Healthcare Products Co. Div.Of Tyco Health Filter by specialty or product code using the sidebar.
66 devices
Cleared
Dec 31, 1997
KENDALL CURITY IODOFORM PACKING STRIP
General & Plastic Surgery
90d
Cleared
Dec 16, 1997
KENDALL CURITY PETROLATUM GAUZE
General & Plastic Surgery
90d
Cleared
Dec 15, 1997
KENDALL XEROFORM PETROLATUM DRESSING (6311,6312,6313,6314,6315,6316,6317)
General & Plastic Surgery
90d
Cleared
Dec 10, 1997
KENDALL CURITY NON-ADHERING DRESSING
General & Plastic Surgery
78d
Cleared
Dec 04, 1997
KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSING
General & Plastic Surgery
79d
Cleared
Nov 07, 1997
KENDALL FAST-CATH PRE LUBRICATED URETHRAL CATHETER
Gastroenterology & Urology
50d
Cleared
Apr 23, 1997
KENDALL HYDROPHILIC POWDER WOUND DRESSING
General & Plastic Surgery
90d
Cleared
Mar 18, 1997
KENDALL DUAL LUMEN CATHETER
Gastroenterology & Urology
196d
Cleared
Feb 07, 1997
KENDALL CURITY URETERAL CATHETER
Gastroenterology & Urology
66d
Cleared
Dec 20, 1996
CURITY THORACENTESIS TRAY
General Hospital
38d
Cleared
Jul 31, 1996
KENDALL SHER-I-BRONCH ENDOBROCHIAL TUBE
Anesthesiology
72d
Cleared
May 30, 1996
KENDALL BLUNT TUOHY EPIDURAL NEEDLE
Anesthesiology
231d
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