Submission Details
| 510(k) Number | K213551 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 08, 2021 |
| Decision Date | March 02, 2022 |
| Days to Decision | 114 days |
| Submission Type | Traditional |
| Review Panel | General Hospital (HO) |
| Summary | Summary PDF |
K213551 is an FDA 510(k) clearance for the Giraffe Omnibed Carestation CS1, a Warmer, Infant Radiant (Class II — Special Controls, product code FMT), submitted by Datex-Ohmeda, Inc. (Wauwatosa, US). The FDA issued a Cleared decision on March 2, 2022, 114 days after receiving the submission on November 8, 2021. This device falls under the General Hospital review panel. Regulated under 21 CFR 880.5130.
| 510(k) Number | K213551 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 08, 2021 |
| Decision Date | March 02, 2022 |
| Days to Decision | 114 days |
| Submission Type | Traditional |
| Review Panel | General Hospital (HO) |
| Summary | Summary PDF |
| Product Code | FMT — Warmer, Infant Radiant |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 880.5130 |