5 MHZ INTRACAVITARY PROBE, MODEL H4222V— 510(k) K860233
Substantially EquivalentGeneral Electric Co.
FDA 510(k) clearance K860233 for 5 MHZ INTRACAVITARY PROBE, MODEL H4222V, Substantially Equivalent on 1986-06-02. 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.