UROLOGIX TARGIS SYSTEM
FDA premarket approval P970008/S046 · decided 2009-10-22
Approval details
- PMA number
- P970008
- Supplement
- S046
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- UROLOGIX TARGIS SYSTEM
- Generic name
- System, hyperthermia, rf/microwave (benign prostatic hyperplasia),thermotherapy
- Applicant
- Urologix, LLC
- Date received
- 2009-09-23
- Decision date
- 2009-10-22
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- MEQ
- Advisory committee
- Gastroenterology, Urology
- Expedited review
- No
- Location
- Plymouth, MN
- Statement
- RELOCATION OF AN IN-PROCESS TEST FOR A COMPONENT FROM THE CONTROLLED ENVIRONMENT AREA TO ANOTHER IN-PROCESS ROOM.
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