510(k) K203426
K203426 is an FDA 510(k) premarket notification submitted by Nantong Taiweishi Medical Technology Co., Ltd. for the device "Surgical Face Mask (non-sterile)". The FDA issued a decision of Substantially Equivalent on Feb 18, 2021. The device falls under product code FXX (Mask, Surgical), a Class II device regulated under 21 CFR 878.4040. Nantong Taiweishi Medical Technology Co., Ltd. has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 18, 2021
- Date Received
- Nov 20, 2020
- 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)