PMA P070022S008
- Device
- ADIANA PERMANENT CONTRACEPTION SYSTEM
- Applicant
- Hologic, Inc.
- PMA number
- P070022
- Supplement
- S008
- Product code
- KNH
- Decision date
- 2011-05-05
- Generic name
- Laparoscopic contraceptive tubal occlusion device
- Approval order statement
- APPROVAL FOR REVISION OF WRIITEN WORK INSTRUCTIONS FOR A SOLDERING OPERATION.
Current openFDA PMA Record
- Device
- ADIANA PERMANENT CONTRACEPTION SYSTEM
- Applicant
- Hologic, Inc.
- PMA number
- P070022
- Supplement
- S008
- Product code
- KNH
- Generic name
- Laparoscopic contraceptive tubal occlusion device
- Decision date
- 2011-05-05
- Decision code
- APPR
- Date received
- 2010-11-19
- Supplement type
- 135 Review Track For 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL FOR REVISION OF WRIITEN WORK INSTRUCTIONS FOR A SOLDERING OPERATION.