510(k) K203012
K203012 is an FDA 510(k) premarket notification submitted by Customfab, Inc. for the device "Surgical Mask". The FDA issued a decision of Substantially Equivalent on Apr 11, 2021. The device falls under product code FXX (Mask, Surgical), a Class II device regulated under 21 CFR 878.4040.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 11, 2021
- Date Received
- Oct 1, 2020
- Clearance Type
- Abbreviated
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Mask, Surgical
- Device Class
- Class II
- Regulation Number
- 878.4040
- Review Panel
- HO
- Submission Type
- 510(k)