Radius Intl., Inc.
Radius Intl., Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 23, 1998.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K972025 | RADIUS PULL PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT | January 23, 1998 |
| K972102 | RADIUS PUSH OVER THE GUIDE WIRE PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT | January 23, 1998 |
| K971901 | RADIUS LOW PROFILE GASTROSTOMY TUBE KIT | January 22, 1998 |
| K951560 | RADIUS MANUAL WHWWLCHAIRS (COBRA, VIPER, SWING, OLYMPIA, AND MOBIL MODELS) | April 17, 1995 |
| K930510 | RADIUS ENTERAL FEEDING TUBE | February 1, 1995 |