FDA 510(k) Applications Submitted by AMERTEK MEDICAL, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K030518 | 02/19/2003 | AMERITEK SURE-POINT TRACKER SYSTEM | AMERTEK MEDICAL, INC. |
| K031273 | 04/22/2003 | AMERITEK SURE-POINT HDR NEEDLE TEMPLATE | AMERTEK MEDICAL, INC. |
| K011581 | 05/23/2001 | AMERITEK BRACHYTHERAPY TEMPLATE | AMERTEK MEDICAL, INC. |
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