K212264 is an FDA 510(k) clearance for the Surgical Face mask. This device is classified as a Mask, Surgical (Class II - Special Controls, product code FXX).
Submitted by Nantong Taiweishi Medical Technology Co., Ltd. (Nantong, CN). The FDA issued a Cleared decision on November 13, 2021, 116 days after receiving the submission on July 20, 2021.
This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 878.4040.
| 510(k) Number | K212264 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 20, 2021 |
| Decision Date | November 13, 2021 |
| Days to Decision | 116 days |
| Submission Type | Traditional |
| Review Panel | General Hospital (HO) |
| Summary | Summary PDF |
| Product Code | FXX - Mask, Surgical |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.4040 |