FDA 510(k) Applications Submitted by MAX STURGIS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K991989 | 06/14/1999 | MITAKA POINT SETTER | MITAKA USA, INC. |
| K061871 | 07/03/2006 | LEICA MODEL FL800 | LEICA MICROSYSTEMS, INC. |
| K984355 | 12/07/1998 | POINT SETTER | MITAKA USA, INC. |
| K090792 | 03/24/2009 | MITAKA UNIARM | MITAKA KOHKI CO., LTD. |
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