FDA 510(k) Applications Submitted by MICHAEL A DOUGLAS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K160121 | 01/19/2016 | CorPath GRX System | Corindus, Inc. |
| K080098 | 01/14/2008 | MRJ EXTENDED | PARAMED SRL |
| K001773 | 06/12/2000 | ORTHONE | ONI, INC. |
| K052698 | 09/28/2005 | MODIFICATION TO: AURORA | AURORA IMAGING TECHNOLOGY, INC. |
| K073362 | 11/30/2007 | MROPEN | PARAMED SRL |
| K073425 | 12/03/2007 | MODIFICATION TO AURORA MRI SYSTEM | AURORA IMAGING TECHNOLOGY, INC. |
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