Submission Details
| 510(k) Number | K232806 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | September 12, 2023 |
| Decision Date | June 07, 2024 |
| Days to Decision | 269 days |
| Submission Type | Traditional |
| Review Panel | General Hospital (HO) |
| Summary | Summary PDF |
K232806 is an FDA 510(k) clearance for the HALYARD* FLUIDSHIELD* 1 Procedure Mask with So Soft Lining and So Soft Earloops (25867); HALYARD* Level 1 Procedure Mask (48388), a Mask, Surgical (Class II — Special Controls, product code FXX), submitted by Owens & Minor (O&M) Halyard, Inc. (Mechanicsville, US). The FDA issued a Cleared decision on June 7, 2024, 269 days after receiving the submission on September 12, 2023. This device falls under the General Hospital review panel. Regulated under 21 CFR 878.4040.
| 510(k) Number | K232806 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | September 12, 2023 |
| Decision Date | June 07, 2024 |
| Days to Decision | 269 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 |