Atlas FDA

Ampere™ Generator

FDA premarket approval P060019/S054 · decided 2021-10-14

Approval details

PMA number
P060019
Supplement
S054
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Ampere™ Generator
Generic name
catheter, percutaneous, cardiac ablation, for treatment of atrial flutter
Applicant
Irvine Biomedical, Inc.
Date received
2021-09-14
Decision date
2021-10-14
Days to decision
30 days
Decision code
OK30
Product code
OAD
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
Implement non-product software changes to the Ampere Generator and Remote Control Calibration and Functional Tests, and the Best Electrical Automated Safety Tester (BEAST) electrical test processes involved in the manufacture of Ampere Generator and Remote Control.

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510(k) clearances by this applicant

RecordFirmDate
INQUIRY H-CURVE TV STEERABLE DIAGNOSTIC CATHETER (K082061)Irvine Biomedical, Inc.2008-08-19
INQUIRY OPTIMA PLUS STEERABLE ELECTROPHYSIOLOGY CATHETER (K060757)Irvine Biomedical, Inc.2006-04-19
INQUIRY AFOCUS II DIAGNOSTIC CATHETER (K053582)Irvine Biomedical, Inc.2006-03-21
INQUIRY AFOCUS, INQUIRY AFOCUS II AND INQUIRY OPTIMA STEERABLE ELECTROPHYSIOLOGY CATHETER (K042775)Irvine Biomedical, Inc.2004-11-04
AFOCUS ELECTROPYSIOLOGY CATHETER SYSTEM, MODELS 81550, 81567, 81568, 81569 (K010471)Irvine Biomedical, Inc.2001-06-06
LUMA-CATH STEERABLE EP CATHETERS (K991878)Irvine Biomedical, Inc.1999-12-10
LUMA-CATH FIXED CURVE EP CATHETERS (K991025)Irvine Biomedical, Inc.1999-10-15
ORTHOGONAL EP CATHETERS (K990958)Irvine Biomedical, Inc.1999-06-03