MPX 80— 510(k) K770006
Substantially EquivalentGeneral Electric Co.
FDA 510(k) clearance K770006 for MPX 80, Substantially Equivalent on 1977-01-18. Applicant: General Electric Co.. Device class: 1.
Clearance details
- Applicant
- General Electric Co.
- Product code
- Code IZO
- Device class
- Class 1
- Regulation
- 21 CFR 892.1700
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code IZO
view allMore clearances from General Electric Co.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.