FDA 510(k) Applications Submitted by RONALD D WOLFE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K031630 | 05/27/2003 | BIFURCATED ALLERGY SKIN TESTING NEEDLE | PRECISION MEDICAL PRODUCTS, INC. |
| K012515 | 08/06/2001 | BIFURCATED VACCINATING NEEDLE | PRECISION MEDICAL PRODUCTS, INC. |
| K955413 | 11/27/1995 | ENDOVATIONS TRIPLE LUMEN BALLOON DILATATION CATHETER | ENDOVATIONS |
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