FDA 510(k) Applications Submitted by Spaulding Clinical Research, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K150564 | 03/06/2015 | Spaulding Electrocardiograph 2100iQ | Spaulding Clinical Research, LLC |
| K110065 | 01/10/2011 | SPAULDING IQ ELECTROCARDIOGRAPH | SPAULDING CLINICAL RESEARCH, LLC |
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