PMA P920046S005
- Device
- FEMCARE FILSHIE CLIP SYSTEM
- Applicant
- Femcare , Ltd.
- PMA number
- P920046
- Supplement
- S005
- Product code
- KNH
- Decision date
- 2008-05-15
- Classification
- Laparoscopic Contraceptive Tubal Occlusion Device
- Generic name
- Laparoscopic contraceptive tubal occlusion device
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE LOCATED AT WESLEY COE LTD., ENGLAND, UNITED KINGDOM.
Current openFDA PMA Record#
- Device
- FEMCARE FILSHIE CLIP SYSTEM
- Applicant
- Femcare , Ltd.
- PMA number
- P920046
- Supplement
- S005
- Product code
- KNH
- Generic name
- Laparoscopic contraceptive tubal occlusion device
- Decision date
- 2008-05-15
- Decision code
- APPR
- Date received
- 2008-04-14
- 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 WESLEY COE LTD., ENGLAND, UNITED KINGDOM.