510(k) K210970
K210970 is an FDA 510(k) premarket notification submitted by Byd Precison Manufacturer Co., Ltd. for the device "Single-Use Surgical Mask Model FE2311B". The FDA issued a decision of Substantially Equivalent on Jul 21, 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
- Jul 21, 2021
- Date Received
- Mar 31, 2021
- Clearance Type
- Traditional
- 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)