PMA P110014S003
- Device
- MARGINPROBE SYSTEM
- Applicant
- Dilon Medical Technologies, Ltd.
- PMA number
- P110014
- Supplement
- S003
- Product code
- OEE
- Decision date
- 2014-09-24
- Classification
- Diagnostic Low Electric Field
- Generic name
- Diagnostic low electric field
- Approval order statement
- APPROVAL FOR THE MODIFICATION MADE TO THE MARGINPROBE CONSOLE FROMMARGINPROBE TYPE 1.1 TO MARGINPROBE TYPE 1.2.
Current openFDA PMA Record#
- Device
- MARGINPROBE SYSTEM
- Applicant
- Dilon Medical Technologies, Ltd.
- PMA number
- P110014
- Supplement
- S003
- Product code
- OEE
- Generic name
- Diagnostic low electric field
- Decision date
- 2014-09-24
- Decision code
- APPR
- Date received
- 2014-04-15
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Approval order statement
- APPROVAL FOR THE MODIFICATION MADE TO THE MARGINPROBE CONSOLE FROMMARGINPROBE TYPE 1.1 TO MARGINPROBE TYPE 1.2.