5.0 MHZ INTRACAVITARY SECTOR PROBE— 510(k) K853711
Substantially EquivalentGeneral Electric Co.
FDA 510(k) clearance K853711 for 5.0 MHZ INTRACAVITARY SECTOR PROBE, Substantially Equivalent on 1985-12-18. Applicant: General Electric Co..
Clearance details
- Applicant
- General Electric Co.
- Product code
- Code HEM
- Advisory panel
- Obstetrics/Gynecology
- 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.