FDA 510(k) Applications Submitted by SurgEase Innovations Limited
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K232262 | 07/31/2023 | LumenEye« X1 endoscope (LX1-SCP-203); LumenEye« X1 consumables (LX1-CSB-201); LumenEye« X1 Consumable Carton (25 Sets) (LX1-CSP-201 ) | SurgEase Innovations Limited |
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