The Kendall Company is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Kendall Company - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
The Kendall Company has 8 FDA 510(k) cleared medical devices. Based in Mansfield, US.
Historical record: 8 cleared submissions from 2001 to 2006. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by The Kendall Company Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Kendall Company
8 devices
Cleared
Aug 09, 2006
KENDALL ARGYLE NEONATAL/PEDIATRIC PICC, MODEL 43311
General Hospital
30d
Cleared
May 13, 2003
MAHURKAR OPLUS CATHETER, MODEL 13.5 FR
Gastroenterology & Urology
112d
Cleared
Apr 10, 2002
MAHURKAR TRIPLE LUMEN CATHETER, 12 FR
Gastroenterology & Urology
90d
Cleared
Oct 15, 2001
MONOJECT PREFILL 0.9% SODIUM CHLORIDE FLUSH SYRINGE
General Hospital
171d
Cleared
Aug 22, 2001
EXCILON AMD ANTIMICROBIAL SPONGE MODEL #7088
General & Plastic Surgery
62d
Cleared
Apr 09, 2001
TANDEM-CATH 10 FR. CATHETER SYSTEM, MODEL MULTIPLE CODE NUMBERS
Gastroenterology & Urology
203d
Cleared
Mar 28, 2001
KENDALL 14.5 FR MAXID CUFFED DUAL LUMEN CATHETER
Gastroenterology & Urology
191d
Cleared
Jan 11, 2001
FILAC FAS TEMP ELECTRONIC THERMOMETER
General Hospital
80d