PMA P990025S072

Device
nMARQ Catheter Interference Cable
Applicant
Biosense Webster, Inc.
PMA number
P990025
Supplement
S072
Product code
DRF
Decision date
2024-11-15
Classification
Cardiovascular
Generic name
CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING
Approval order statement
an alternate manufacturing site located in Tijuana, Baja California, Mexico (Establishment Registration Number 3008093809) for the TX eco EXT Cable, nMARQ Catheter Interface Cable, and the SmartAblate System Interface Cable

Current openFDA PMA Record#

Device
nMARQ Catheter Interference Cable
Applicant
Biosense Webster, Inc.
PMA number
P990025
Supplement
S072
Product code
DRF
Generic name
CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING
Decision date
2024-11-15
Decision code
APPR
Date received
2024-03-12
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
an alternate manufacturing site located in Tijuana, Baja California, Mexico (Establishment Registration Number 3008093809) for the TX eco EXT Cable, nMARQ Catheter Interface Cable, and the SmartAblate System Interface Cable