Pure EP

FDA 510(k) K180805 · Biosig Technologies

Substantially Equivalent

510(k) numberK180805

Submission

Device name
Pure EP
Applicant
Biosig Technologies
Los Angeles, CA, US
Received
March 28, 2018
Decision date
August 8, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DQK – Computer, Diagnostic, Programmable
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1425
Specialty
Cardiovascular

Other 510(k)s with product code DQK

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K262005Affera Integrated Mapping SystemDQK · Special Medtronic, Inc.08/21/2026SE
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K253576CorVista System® with PCWP Add-OnDQK · Traditional Analytics For Life, Inc.07/26/2026SE
K262006EnSite™ X EP SystemDQK · Special Abbott Medical07/15/2026SE
K252978ScioCardio ECG Analysis PlatformDQK · Traditional Synergen Technology Labs, LLC07/09/2026SE
K253463ILR ECG Analyzer (IM007)DQK · Traditional Implicity, Inc.07/02/2026SE
K261119NorthStar Mapping System (MAP01 or MAP01-01)DQK · Special Imricor Medical Systems, Inc.06/30/2026SE
K253088OneStim-DUO Cardiac Stimulator (MP5003-4CO)DQK · Traditional Micropace Pty, Ltd.06/12/2026SE
K261329Intra-Operative Positioning System (IOPS) (MC-1);IOPS Viewpoint Simple Curve Catheter…DQK · Special Centerline Biomedical06/10/2026SE
K252859ZEUS Platform (FG0501US)DQK · Traditional iRhythm Technologies, Inc.05/29/2026SE

Questions and answers

When was Pure EP cleared by the FDA?

Pure EP (K180805) received a 510(k) decision of Substantially Equivalent on August 8, 2018, 133 days after the submission was received.

What is the product code of K180805?

The FDA product code is DQK – Computer, Diagnostic, Programmable, a Class II (moderate risk) device regulated under 21 CFR 870.1425.