PMA P010068S025
- Device
- CELSIUS & NAVISTAR DS CATHETER/NAVISTAR RMT/EZ STEER NAV/QWIKSTAR DS CATHETER/INTERFACE CABLES
- Applicant
- Biosense Webster, Inc.
- PMA number
- P010068
- Supplement
- S025
- Product code
- OAD
- Decision date
- 2011-10-07
- Classification
- Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
- Generic name
- catheter, percutaneous, cardiac ablation, for treatment of atrial flutter
- Approval order statement
- PARAMETRIC RELEASE OF STERILIZED PRODUCT USING ETHYLENE OXIDE.
Current openFDA PMA Record#
- Device
- CELSIUS & NAVISTAR DS CATHETER/NAVISTAR RMT/EZ STEER NAV/QWIKSTAR DS CATHETER/INTERFACE CABLES
- Applicant
- Biosense Webster, Inc.
- PMA number
- P010068
- Supplement
- S025
- Product code
- OAD
- Generic name
- catheter, percutaneous, cardiac ablation, for treatment of atrial flutter
- Decision date
- 2011-10-07
- Decision code
- OK30
- Date received
- 2011-08-29
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- PARAMETRIC RELEASE OF STERILIZED PRODUCT USING ETHYLENE OXIDE.