FDA 510(k) Applications Submitted by THE NEWMAN GROUP, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K090465 | 02/23/2009 | DIGDOP ULTRASOUND SYSTEM | THE NEWMAN GROUP, LLC |
| K061091 | 04/19/2006 | BABYBEAT CORDLESS | THE NEWMAN GROUP, LLC |
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