Medical Devices/Padpro, Inc.
1 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| DEFIBRILLATOR CABLE TESTER, MODEL DT2200 (K061606) | Medical Devices/Padpro, Inc. | 2006-06-21 |
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Every clearance here is in the API, with alerts when new ones post.