D-Laser Blue, D-Laser 16— 510(k) K210367
Substantially EquivalentGuilin Woodpecker Medical Instrument Co., Ltd.
FDA 510(k) clearance K210367 for D-Laser Blue, D-Laser 16, Substantially Equivalent on 2022-03-10. Applicant: Guilin Woodpecker Medical Instrument Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Guilin Woodpecker Medical Instrument Co., Ltd.
- Product code
- Code NVK
- Device class
- Class 2
- Regulation
- 21 CFR 878.4810
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Guilin, CN
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