K242001
- 510(k) number
- K242001
- Device name
- Philips VSC-MEDlib
- Applicant
- Philips Medical Systems Nederland B.V. NL
- Product code
- BZQ — Monitor, Breathing Frequency
- Decision date
- 2025-04-04
- Date received
- 2024-07-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K242001.pdf
Official FDA record: K242001
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.