PMA P950005S087

Device
nMARQ Catheter Interference Cable
Applicant
Biosense Webster, Inc.
PMA number
P950005
Supplement
S087
Product code
LPB
Decision date
2024-11-15
Classification
Cardiovascular
Generic name
Cardiac ablation percutaneous catheter
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
P950005
Supplement
S087
Product code
LPB
Generic name
Cardiac ablation percutaneous catheter
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