Tri-Med Specialties, Inc.
Tri-Med Specialties, Inc. holds FDA 510(k) medical device clearances, first cleared 1985, most recent 1997.
Top product codes for Tri-Med Specialties, Inc.
Recent clearances by Tri-Med Specialties, Inc.
- K971615 — PATTISON ESOPHAGEAL DILATOR
- K970890 — #ES-32 SUCTION CATHETER 32 FR.
- K970982 — T-RX RETRIEVAL FORCEPS
- K942918 — TRI-MED ENDOSCOPIC FLUID INTRODUCTION CATHETER
- K950574 — NEEDLE/CANNULA
- K934348 — TRI-MED QUICK-STEP GASTRIC LAVAGE TUBE SIZES 18FR, 22FR, 32FR
- K945160 — PARACENTESIS NEEDLES/CANNULAS
- K924549 — TRI-MED QUICK-STEP(TM) RECTAL TUBE
- K932015 — TRI-MED INFLATABLE ESOPHAGEAL DILATOR
- K932652 — TRI-MED PARACENTESIS TRAY
- K931201 — TRI-MED ENDOSCOPIC FLUID INTRODUCTION CATHETER
- K920527 — TRI-MED QUICK-STEP GASTRIC LAVAGE KIT
- K920619 — TRI-MED GASTRIC LAVAGE SYSTEM
- K852535 — E-Z P.E.G. W/PERCUTANEOUS ENDOSCOPY GASTROSTOMY
Data sourced from openFDA. This site is unofficial and independent of the FDA.