INTRAOPERATIVE RADIATION THERAPY DEVICES— 510(k) K891261
Substantially EquivalentGeneral Electric Co.
FDA 510(k) clearance K891261 for INTRAOPERATIVE RADIATION THERAPY DEVICES, Substantially Equivalent on 1989-04-26. Applicant: General Electric Co..
Clearance details
- Applicant
- General Electric Co.
- Product code
- Code LHN
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Milwaukee, WI, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.