Medical Diode Laser Systems (GBOX-6H, GBOX-10D , GBOX-12D, GBOX-15D, VELAS Pro-30B15D, VELAS II-6H, VELAS II-15D)
FDA 510(k) clearance K241791 · decided 2025-03-19
Clearance details
- K-number
- K241791
- Device name
- Medical Diode Laser Systems (GBOX-6H, GBOX-10D , GBOX-12D, GBOX-15D, VELAS Pro-30B15D, VELAS II-6H, VELAS II-15D)
- Applicant
- Gigaalaser Company , Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2024-06-21
- Decision date
- 2025-03-19
- Days to decision
- 271 days
- Clearance type
- Traditional
- Product code
- GEX
- Device class
- 2
- Regulation number
- 878.4810
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Wu Han, CN
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.