PMA P970008S007
- Device
- UROLOGIC TARGIS SYSTEM
- Applicant
- Urologix, LLC
- PMA number
- P970008
- Supplement
- S007
- Product code
- MEQ
- Decision date
- 1998-07-07
- Classification
- System, Hyperthermia, Rf/microwave (benign Prostatic Hyperplasia),thermotherapy
- Generic name
- System, hyperthermia, rf/microwave (benign prostatic hyperplasia),thermotherapy
- Approval order statement
- Approval for the Targis(TM) Patient Comfort Kit which includes the MDS Holder and Knee Cusions.
Current openFDA PMA Record#
- Device
- UROLOGIC TARGIS SYSTEM
- Applicant
- Urologix, LLC
- PMA number
- P970008
- Supplement
- S007
- Product code
- MEQ
- Generic name
- System, hyperthermia, rf/microwave (benign prostatic hyperplasia),thermotherapy
- Decision date
- 1998-07-07
- Decision code
- APPR
- Date received
- 1998-06-30
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Approval order statement
- Approval for the Targis(TM) Patient Comfort Kit which includes the MDS Holder and Knee Cusions.