FDA 510(k) Applications Submitted by RADIUS INTL., INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K971901 | 05/23/1997 | RADIUS LOW PROFILE GASTROSTOMY TUBE KIT | RADIUS INTL., INC. |
| K972025 | 06/02/1997 | RADIUS PULL PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT | RADIUS INTL., INC. |
| K972102 | 06/04/1997 | RADIUS PUSH OVER THE GUIDE WIRE PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT | RADIUS INTL., INC. |
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