FDA 510(k) Applications Submitted by PREMIER HEART, LLC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K992703 | 08/12/1999 | CARDIOTRON EKG MULTI-PHASE INFORMATION ANALYSIS SYSTEM, MODELS 3800, 6800, 8800 | PREMIER HEART, LLC. |
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