PMA P070022S025
- Device
- ADIANA CONTRACEPTION SYSTEM
- Applicant
- Hologic, Inc.
- PMA number
- P070022
- Supplement
- S025
- Product code
- KNH
- Decision date
- 2012-03-20
- Generic name
- Laparoscopic contraceptive tubal occlusion device
- Approval order statement
- APPROVAL FOR MODIFICATIONS OF THE ADIANA RF GENERATOR TO INCORPORATE A TOUCH SCREEN USER INTERFACE.
Current openFDA PMA Record#
- Device
- ADIANA CONTRACEPTION SYSTEM
- Applicant
- Hologic, Inc.
- PMA number
- P070022
- Supplement
- S025
- Product code
- KNH
- Generic name
- Laparoscopic contraceptive tubal occlusion device
- Decision date
- 2012-03-20
- Decision code
- APPR
- Date received
- 2012-01-11
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Approval order statement
- APPROVAL FOR MODIFICATIONS OF THE ADIANA RF GENERATOR TO INCORPORATE A TOUCH SCREEN USER INTERFACE.