Shotwell & Carr, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K970824 | MDX 2000, DIGITAL ANALYZER | JOY | 1997-05-30 | View |
| 510(k) | K961011 | DTX-200 BONE DENSITOMETER | KGI | 1996-07-05 | View |
| 510(k) | K950617 | SMART WAVE GS100 | IPF | 1995-10-13 | View |
No matching devices.
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