Atlas FDA

Ampere Generator

FDA premarket approval P110016/S095 · decided 2026-08-07

Approval details

PMA number
P110016
Supplement
S095
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Ampere Generator
Generic name
catheter, percutaneous, cardiac ablation, for treatment of atrial flutter
Applicant
ABBOTT MEDICAL
Date received
2026-05-11
Decision date
2026-08-07
Days to decision
88 days
Decision code
APPR
Product code
OAD
Advisory committee
Cardiovascular
Expedited review
No
Location
Plymouth, MN
Statement
approval for firmware changes to the TactiSys Quartz Equipment v1.8.0 and Ampere Generator v1.2.0 to maintain compatibility with the TactiFlex Duo Ablation Catheter, Sensor Enabled™

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