Radius Intl., Inc.
Radius Intl., Inc. holds FDA 510(k) medical device clearances, first cleared 1995, most recent 1998.
Top product codes for Radius Intl., Inc.
Recent clearances by Radius Intl., Inc.
- K972025 — RADIUS PULL PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT
- K972102 — RADIUS PUSH OVER THE GUIDE WIRE PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT
- K971901 — RADIUS LOW PROFILE GASTROSTOMY TUBE KIT
- K951560 — RADIUS MANUAL WHWWLCHAIRS (COBRA, VIPER, SWING, OLYMPIA, AND MOBIL MODELS)
- K930510 — RADIUS ENTERAL FEEDING TUBE
Data sourced from openFDA. This site is unofficial and independent of the FDA.