Submission Details
| 510(k) Number | K212200 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 14, 2021 |
| Decision Date | October 22, 2021 |
| Days to Decision | 100 days |
| Submission Type | Traditional |
| Review Panel | General Hospital (HO) |
| Summary | Summary PDF |
K212200 is an FDA 510(k) clearance for the STERLINKTM FPS-15s Plus Sterilizer with STERLOADTM Cassette, a Sterilizer, Chemical (Class II — Special Controls, product code MLR), submitted by Plasmapp Co,., Ltd. (Daejeon, KR). The FDA issued a Cleared decision on October 22, 2021, 100 days after receiving the submission on July 14, 2021. This device falls under the General Hospital review panel. Regulated under 21 CFR 880.6860.
| 510(k) Number | K212200 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 14, 2021 |
| Decision Date | October 22, 2021 |
| Days to Decision | 100 days |
| Submission Type | Traditional |
| Review Panel | General Hospital (HO) |
| Summary | Summary PDF |
| Product Code | MLR — Sterilizer, Chemical |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 880.6860 |