HeartLight System

FDA Premarket Approval P150026 S009

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

To increase the load size in the existing sterilization process

DeviceHeartLight System
Generic NameCatheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
ApplicantCARDIOFOCUS, INC.
Date Received2019-12-18
Decision Date2020-01-16
PMAP150026
SupplementS009
Product CodeOAE 
Advisory CommitteeCardiovascular
Supplement Type30-day Notice
Supplement ReasonProcess Change - Manufacturer/sterilizer/packager/supplier
Expedited ReviewNo
Combination Product No
Applicant Address CARDIOFOCUS, INC. 500 Nickerson Road marlborough, MA 01752

Supplemental Filings

Supplement NumberDateSupplement Type
P150026Original Filing
S009 2019-12-18 30-day Notice
S008
S007 2019-08-13 Real-time Process
S006 2019-05-29 Special (immediate Track)
S005 2019-01-08 Normal 180 Day Track
S004 2018-04-04 30-day Notice
S003 2017-11-09 Real-time Process
S002 2017-08-09 Normal 180 Day Track
S001 2017-05-05 Real-time Process

NIH GUDID Devices

Device IDPMASupp
00868976000178 P150026 000
00868976000161 P150026 000
00868976000154 P150026 000
00868976000130 P150026 000
00868976000123 P150026 000
00868976000116 P150026 000
00868976000109 P150026 000

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