FDA 510(k) Applications Submitted by MATTIOLI ENGINEERING CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K100053 | 01/08/2010 | MATTIOLI PULSE TWO/THREE PLUS FAMILY | MATTIOLI ENGINEERING CORP. |
| K032968 | 09/23/2003 | TRSANSDERM IONTO SYSTEM | MATTIOLI ENGINEERING CORP. |
| K042590 | 09/23/2004 | TRANSDERM IONTO SYSTEM, MK 2 | MATTIOLI ENGINEERING CORP. |
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