The Newman Group, LLC
2 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| DIGDOP ULTRASOUND SYSTEM (K090465) | The Newman Group, LLC | 2009-04-08 |
| BABYBEAT CORDLESS (K061091) | The Newman Group, LLC | 2006-05-04 |
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