PMA P990025S054
- Device
- NaviStar Catheter
- Applicant
- Biosense Webster, Inc.
- PMA number
- P990025
- Supplement
- S054
- Product code
- DRF
- Decision date
- 2017-10-10
- Classification
- Catheter, Electrode Recording, Or Probe, Electrode Recording
- Generic name
- CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING
- Approval order statement
- Transfer of the extrusion process of the Braided Dual Lumen and Braided Triple Lumen subcomponent catheter part.
Current openFDA PMA Record#
- Device
- NaviStar Catheter
- Applicant
- Biosense Webster, Inc.
- PMA number
- P990025
- Supplement
- S054
- Product code
- DRF
- Generic name
- CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING
- Decision date
- 2017-10-10
- Decision code
- OK30
- Date received
- 2017-09-11
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Transfer of the extrusion process of the Braided Dual Lumen and Braided Triple Lumen subcomponent catheter part.