Atlas FDA

Therapy Dual 8 Ablation Catheters

FDA premarket approval P040042/S036 · decided 2016-09-08

Approval details

PMA number
P040042
Supplement
S036
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Therapy Dual 8 Ablation Catheters
Generic name
catheter, percutaneous, cardiac ablation, for treatment of atrial flutter
Applicant
Irvine Biomedical,Inc.(Ibi)
Date received
2016-08-12
Decision date
2016-09-08
Days to decision
27 days
Decision code
OK30
Product code
OAD
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
Changes to the environmental specifications and installation of data loggers for environmental monitoring.

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510(k) clearances by this applicant

RecordFirmDate
IBI INQUIRY CLEARICE INTRACARDIAC ECHOCARDIOGRAPHY ULTRASOUND IMAGING CATHETER (K070011)Irvine Biomedical,Inc.(Ibi)2007-03-20