Livocare Surgical Mask
FDA 510(k) clearance K201380 · decided 2020-10-07
Clearance details
- K-number
- K201380
- Device name
- Livocare Surgical Mask
- Applicant
- Andon Health Co, Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2020-05-26
- Decision date
- 2020-10-07
- Days to decision
- 134 days
- Clearance type
- Abbreviated
- Product code
- FXX
- Device class
- 2
- Regulation number
- 878.4040
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Tianjin, CN
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.