PMA P110014S002
- Device
- MARGINPROBE SYSTEM
- Applicant
- Dilon Medical Technologies, Ltd.
- PMA number
- P110014
- Supplement
- S002
- Product code
- OEE
- Decision date
- 2014-05-15
- Classification
- Diagnostic Low Electric Field
- Generic name
- Diagnostic low electric field
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE LOCATED AT MEDIMOR LTD., IN TIBERIAS, ISRAEL (CONTRACT MANUFACTURER).
Current openFDA PMA Record#
- Device
- MARGINPROBE SYSTEM
- Applicant
- Dilon Medical Technologies, Ltd.
- PMA number
- P110014
- Supplement
- S002
- Product code
- OEE
- Generic name
- Diagnostic low electric field
- Decision date
- 2014-05-15
- Decision code
- APPR
- Date received
- 2014-01-28
- Supplement type
- Normal 180 Day Track No User Fee
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE LOCATED AT MEDIMOR LTD., IN TIBERIAS, ISRAEL (CONTRACT MANUFACTURER).