PMA P970008S002
- Device
- UROLOGIC TARGIS SYSTEM
- Applicant
- Urologix, LLC
- PMA number
- P970008
- Supplement
- S002
- Product code
- MEQ
- Decision date
- 1998-01-09
- 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 new manufacturing facility located at SeaMED Corp., 21621 30th ave., NE, Bothell, WA 98021.
Current openFDA PMA Record#
- Device
- UROLOGIC TARGIS SYSTEM
- Applicant
- Urologix, LLC
- PMA number
- P970008
- Supplement
- S002
- Product code
- MEQ
- Generic name
- System, hyperthermia, rf/microwave (benign prostatic hyperplasia),thermotherapy
- Decision date
- 1998-01-09
- Decision code
- APPR
- Date received
- 1997-09-05
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Approval for a new manufacturing facility located at SeaMED Corp., 21621 30th ave., NE, Bothell, WA 98021.