Single-use Medical Face Mask
FDA 510(k) clearance K203591 · decided 2021-07-02
Clearance details
- K-number
- K203591
- Device name
- Single-use Medical Face Mask
- Applicant
- Conod Medical Co., Limited
- Decision
- Substantially Equivalent
- Date received
- 2020-12-08
- Decision date
- 2021-07-02
- Days to decision
- 206 days
- Clearance type
- Traditional
- Product code
- FXX
- Device class
- 2
- Regulation number
- 878.4040
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Changshu, CN
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.