K240271
- 510(k) number
- K240271
- Device name
- Linshom Continuous Predictive Respiratory Monitoring System (CPRMS)
- Applicant
- Linshom Medical, Inc. MD · US
- Product code
- BZQ — Monitor, Breathing Frequency
- Decision date
- 2024-09-11
- Date received
- 2024-01-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
510(k) Summary (official FDA PDF): K240271.pdf
Official FDA record: K240271
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.