PicoLO Nd:YAG Picosecond Laser System
FDA 510(k) clearance K183392 · decided 2019-01-04
Clearance details
- K-number
- K183392
- Device name
- PicoLO Nd:YAG Picosecond Laser System
- Applicant
- Laseroptek Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2018-12-07
- Decision date
- 2019-01-04
- Days to decision
- 28 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
- Gyeonggido, KR
- Third-party review
- Yes
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.