PMA P070022S002
- Device
- ADIANA PERMANENT CONTRACEPTION SYSTEM
- Applicant
- Hologic, Inc.
- PMA number
- P070022
- Supplement
- S002
- Product code
- KNH
- Decision date
- 2010-04-15
- Generic name
- Laparoscopic contraceptive tubal occlusion device
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE LOCATED AT BIOTEST LABORATORIES, INC.MINNEAPOLIS, MINNESOTA.
Current openFDA PMA Record
- Device
- ADIANA PERMANENT CONTRACEPTION SYSTEM
- Applicant
- Hologic, Inc.
- PMA number
- P070022
- Supplement
- S002
- Product code
- KNH
- Generic name
- Laparoscopic contraceptive tubal occlusion device
- Decision date
- 2010-04-15
- Decision code
- APPR
- Date received
- 2010-03-01
- Supplement type
- Normal 180 Day Track No User Fee
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE LOCATED AT BIOTEST LABORATORIES, INC.MINNEAPOLIS, MINNESOTA.