FDA 510(k) Applications Submitted by ReWalk Robotics Ltd. DBA Lifeward
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K241822 | 06/24/2024 | ReWalk« 7 Personal Exoskeleton (50-20-0005) | ReWalk Robotics Ltd. DBA Lifeward |
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