FDA 510(k) Applications Submitted by ACCUTECH MEDICAL TECHNOLOGIES, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K090281 | 02/05/2009 | ACCUTECH FAMILY OF POWERFLEX LASER DELIVERY DEVICES | ACCUTECH MEDICAL TECHNOLOGIES, INC. |
| K061025 | 04/13/2006 | ACCUTECH ENDOLITE PROBE | ACCUTECH MEDICAL TECHNOLOGIES, INC. |
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