FDA 510(k) Applications Submitted by JEROME CANADY
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K052035 | 07/28/2005 | CANADY PLASMA PROBES | CANADY TECHNOLOGY, LLC |
| K212736 | 08/30/2021 | Canady Flex RoboWrist | US Medical Innovations, LLC |
| K113500 | 11/25/2011 | CANADY VIEIRA HYBRID PLASMA SCALPEL | US MEDICAL INNOVATIONS LLC |
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