CARDIAC CATHETERIZATION LAB MONITOR SYS— 510(k) K770179
Substantially EquivalentGeneral Electric Co.
FDA 510(k) clearance K770179 for CARDIAC CATHETERIZATION LAB MONITOR SYS, Substantially Equivalent on 1977-04-05. Applicant: General Electric Co..
Clearance details
- Applicant
- General Electric Co.
- Product code
- Code DXG
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.