K240320
- 510(k) number
- K240320
- Device name
- Patient Monitor (RespArray)
- Applicant
- Edan Instruments, Inc. CN
- Product code
- MHX — Monitor, Physiological, Patient(With Arrhythmia Dete
- Decision date
- 2024-06-28
- Date received
- 2024-02-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.2 MB · U.S. public domain
Also available from FDA: K240320.pdf
Official FDA record: K240320
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.