PMA P920046S009
- Device
- FILSHIE CLIP (MARK VI) SYSTEM
- Applicant
- Femcare , Ltd.
- PMA number
- P920046
- Supplement
- S009
- Product code
- KNH
- Decision date
- 2016-09-09
- Classification
- Laparoscopic Contraceptive Tubal Occlusion Device
- Generic name
- Laparoscopic contraceptive tubal occlusion device
- Approval order statement
- Approval for changing MR Conditional to 3T.
Current openFDA PMA Record#
- Device
- FILSHIE CLIP (MARK VI) SYSTEM
- Applicant
- Femcare , Ltd.
- PMA number
- P920046
- Supplement
- S009
- Product code
- KNH
- Generic name
- Laparoscopic contraceptive tubal occlusion device
- Decision date
- 2016-09-09
- Decision code
- APPR
- Date received
- 2016-03-09
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Approval order statement
- Approval for changing MR Conditional to 3T.