FDA 510(k) Applications Submitted by JAMES R GREENWOOD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K072882 | 10/09/2007 | PAIN VISION, MODEL PS-2100 | OSACHI CO., LTD. |
| K093205 | 10/13/2009 | PADCHECK | PADTEST, LLC |
| K003406 | 11/01/2000 | GUARDED NEEDLE 2000 | INTERNATIONAL MEDICAL DEVICE PARTNERS, INC. |
| K961144 | 03/21/1996 | MS-2000 | TOURITU ENGINEERING CO., INC. |
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