PMA P010055S009
- Device
- PROSTALUND CORETHERM SYSTEM AND PROSTALAND CORETHERM ACCESSORIES
- Applicant
- Prostalund AB
- PMA number
- P010055
- Supplement
- S009
- Product code
- MEQ
- Decision date
- 2014-07-30
- Classification
- System, Hyperthermia, Rf/microwave (benign Prostatic Hyperplasia),thermotherapy
- Generic name
- System, hyperthermia, rf/microwave (benign prostatic hyperplasia),thermotherapy
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE LOCATED AT ORIFICE MEDICAL AB IN YSTAD, SWEDEN.
Current openFDA PMA Record#
- Device
- PROSTALUND CORETHERM SYSTEM AND PROSTALAND CORETHERM ACCESSORIES
- Applicant
- Prostalund AB
- PMA number
- P010055
- Supplement
- S009
- Product code
- MEQ
- Generic name
- System, hyperthermia, rf/microwave (benign prostatic hyperplasia),thermotherapy
- Decision date
- 2014-07-30
- Decision code
- APPR
- Date received
- 2014-02-21
- 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 ORIFICE MEDICAL AB IN YSTAD, SWEDEN.