PMA P070022S014
- Device
- ADIANA PERMANENT CONTRACEPTION SYSTEM
- Applicant
- Hologic, Inc.
- PMA number
- P070022
- Supplement
- S014
- Product code
- KNH
- Decision date
- 2011-09-06
- Generic name
- Laparoscopic contraceptive tubal occlusion device
- Approval order statement
- APPROVAL FOR MINOR CHANGES TO THE SUGAR MOLD MANUFACTURING PROCESS.
Current openFDA PMA Record#
- Device
- ADIANA PERMANENT CONTRACEPTION SYSTEM
- Applicant
- Hologic, Inc.
- PMA number
- P070022
- Supplement
- S014
- Product code
- KNH
- Generic name
- Laparoscopic contraceptive tubal occlusion device
- Decision date
- 2011-09-06
- Decision code
- APPR
- Date received
- 2011-02-28
- Supplement type
- 135 Review Track For 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL FOR MINOR CHANGES TO THE SUGAR MOLD MANUFACTURING PROCESS.