PMA P070022S019
- Device
- ADIANA PERMANENT CONTRACEPTION SYSTEM
- Applicant
- Hologic, Inc.
- PMA number
- P070022
- Supplement
- S019
- Product code
- KNH
- Decision date
- 2011-05-27
- Generic name
- Laparoscopic contraceptive tubal occlusion device
- Approval order statement
- APPROVAL OF A BACKUP STERILIZATION FACILITY LOCATED AT BIOTEST LABORATORIES, INC., IN BROOKLYN PARK, MINNESOTA.
Current openFDA PMA Record
- Device
- ADIANA PERMANENT CONTRACEPTION SYSTEM
- Applicant
- Hologic, Inc.
- PMA number
- P070022
- Supplement
- S019
- Product code
- KNH
- Generic name
- Laparoscopic contraceptive tubal occlusion device
- Decision date
- 2011-05-27
- Decision code
- APPR
- Date received
- 2011-04-13
- Supplement type
- Normal 180 Day Track No User Fee
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL OF A BACKUP STERILIZATION FACILITY LOCATED AT BIOTEST LABORATORIES, INC., IN BROOKLYN PARK, MINNESOTA.