K241556
- 510(k) number
- K241556
- Device name
- Cardiac Workstation (5000); Cardiac Workstation (7000)
- Applicant
- Philips Medizin Systeme Böblingen GmbH DE
- Product code
- DPS — Electrocardiograph
- Decision date
- 2024-12-17
- Date received
- 2024-05-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K241556.pdf
Official FDA record: K241556
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.