FDA 510(k) Applications Submitted by ROBERT BRUCE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K982927 | 08/20/1998 | QUICK TAP SELF DRILLING SCREW | KINAMED, INC. |
| K964362 | 11/01/1996 | KINAMED PROFIX SYSTEM | KINAMED, INC. |
| K002457 | 08/10/2000 | !NSURE FECAL OCCULT BLOOD TEST | ENTERIX INC. |
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