Company ยท US
Radius Intl., Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 1998. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jan 23, 1998 | K972102 | RADIUS PUSH OVER THE GUIDE WIRE PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT Radius Intl., Inc. | KNT |
| Jan 23, 1998 | K972025 | RADIUS PULL PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT Radius Intl., Inc. | KNT |
| Jan 22, 1998 | K971901 | RADIUS LOW PROFILE GASTROSTOMY TUBE KIT Radius Intl., Inc. | KNT |
| Apr 17, 1995 | K951560 | RADIUS MANUAL WHWWLCHAIRS (COBRA, VIPER, SWING, OLYMPIA, AND MOBIL MODELS) Radius Intl., Inc. | IOR |
| Feb 1, 1995 | K930510 | RADIUS ENTERAL FEEDING TUBE Radius Intl., Inc. | BSS |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||