FEMISCAN CLINIC SYSTEM, MODEL FS-ICTRA AND FEMISCAN PERSONAL SYSTEM, MODEL FS-HMTR— 510(k) K993411
Substantially EquivalentMega Electronics , Ltd.
FDA 510(k) clearance K993411 for FEMISCAN CLINIC SYSTEM, MODEL FS-ICTRA AND FEMISCAN PERSONAL SYSTEM, MODEL FS-HMTR, Substantially Equivalent on 2000-01-10. Applicant: Mega Electronics , Ltd..
Clearance details
- Applicant
- Mega Electronics , Ltd.
- Product code
- Code HIR
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- East Longmeadow, MA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.