PMA P970008S040
- Device
- UROLOGIX TARGIX SYSTEM
- Applicant
- Urologix, LLC
- PMA number
- P970008
- Supplement
- S040
- Product code
- MEQ
- Decision date
- 2008-11-19
- Classification
- System, Hyperthermia, Rf/microwave (benign Prostatic Hyperplasia),thermotherapy
- Generic name
- System, hyperthermia, rf/microwave (benign prostatic hyperplasia),thermotherapy
- Approval order statement
- CHANGE OF AN ADHESIVE AND THE TEST METHOD FOR MEASURING TENSILE STRENGTH.
Current openFDA PMA Record#
- Device
- UROLOGIX TARGIX SYSTEM
- Applicant
- Urologix, LLC
- PMA number
- P970008
- Supplement
- S040
- Product code
- MEQ
- Generic name
- System, hyperthermia, rf/microwave (benign prostatic hyperplasia),thermotherapy
- Decision date
- 2008-11-19
- Decision code
- OK30
- Date received
- 2008-10-10
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- CHANGE OF AN ADHESIVE AND THE TEST METHOD FOR MEASURING TENSILE STRENGTH.