K222712
- 510(k) number
- K222712
- Device name
- Fogg System Patient Monitoring Cables
- Applicant
- Fogg System Company, Inc. CO · US
- Product code
- DSA — Cable, Transducer And Electrode, Patient, (Including
- Decision date
- 2023-11-22
- Date received
- 2022-09-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K222712.pdf
Official FDA record: K222712
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.