Tri-Med Specialties, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tri-Med Specialties, Inc. - FDA 510(k) Cleared Devices
14
Total
12
Cleared
0
Denied
Tri-Med Specialties, Inc. has 12 FDA 510(k) cleared gastroenterology & urology devices. Based in Overland Park, US.
Historical record: 12 cleared submissions from 1985 to 1997.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tri-Med Specialties, Inc.
14 devices
Cleared
Jul 24, 1997
PATTISON ESOPHAGEAL DILATOR
Gastroenterology & Urology
83d
Cleared
May 23, 1997
#ES-32 SUCTION CATHETER 32 FR.
Gastroenterology & Urology
73d
Cleared
May 09, 1997
T-RX RETRIEVAL FORCEPS
Gastroenterology & Urology
52d
Cleared
Feb 28, 1995
TRI-MED ENDOSCOPIC FLUID INTRODUCTION CATHETER
Gastroenterology & Urology
252d
Cleared
Feb 24, 1995
NEEDLE/CANNULA
General & Plastic Surgery
28d
Cleared
Dec 23, 1994
TRI-MED QUICK-STEP GASTRIC LAVAGE TUBE SIZES 18FR, 22FR, 32FR
Gastroenterology & Urology
472d
Cleared
Nov 14, 1994
PARACENTESIS NEEDLES/CANNULAS
General & Plastic Surgery
24d
Cleared
Feb 10, 1994
TRI-MED QUICK-STEP(TM) RECTAL TUBE
Gastroenterology & Urology
519d
Cleared
Feb 03, 1994
TRI-MED INFLATABLE ESOPHAGEAL DILATOR
Gastroenterology & Urology
286d
Cleared
Nov 24, 1993
TRI-MED PARACENTESIS TRAY
General & Plastic Surgery
175d
Cleared
Sep 28, 1993
TRI-MED ENDOSCOPIC FLUID INTRODUCTION CATHETER
Gastroenterology & Urology
203d
Cleared
Sep 04, 1992
TRI-MED QUICK-STEP GASTRIC LAVAGE KIT
Gastroenterology & Urology
213d
Cleared
Sep 04, 1992
TRI-MED GASTRIC LAVAGE SYSTEM
Gastroenterology & Urology
206d
Cleared
Oct 17, 1985
E-Z P.E.G. W/PERCUTANEOUS ENDOSCOPY GASTROSTOMY
Gastroenterology & Urology
125d