K223721
- 510(k) number
- K223721
- Device name
- Masimo Stork
- Applicant
- Masimo Corporation CA · US
- Product code
- DQA — Oximeter
- Decision date
- 2023-12-15
- Date received
- 2022-12-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K223721.pdf
Official FDA record: K223721
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.