FDA 510(k) Applications Submitted by REMCO ITALIA S.P.A.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K032200 | 07/18/2003 | ELAN DIGITAL 12 CHANNEL ELECTROCARDIOGRAPH | REMCO ITALIA S.P.A. |
| K032276 | 07/23/2003 | CLICK HOLTER | REMCO ITALIA S.P.A. |
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