FDA 510(k) Applications Submitted by KEPLER MEDTEC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K101660 | 06/14/2010 | ECG SINGLE PATIENT USE LEAD WIRE SET, MODELS 2048801-5 TO 2048801-8 | KEPLER MEDTEC |
| K110462 | 02/17/2011 | KEPLER MEDTEC DISPOSABLE BIPOLAR CABLE | KEPLER MEDTEC |
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