ACCESS POINT TECHNOLOGIES, EP INC.

FDA Device Registration & Listing · Rogers, MN, US · Registration 3005402529

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3005402529
FEI Number
3005402529
Entity Name
ACCESS POINT TECHNOLOGIES, EP INC.
City/State/Country
Rogers, MN, US
Establishment Address
12560 FLETCHER LANE, SUITE 300, Rogers, MN 55374, US
Establishment Type(s)
Manufacture Device in the United States for Export Only
Owner / Operator
Stereotaxis (Owner Number: 9048165)
Owner / Operator Contact Address
710 N. Tucker Blvd., Suite 110, Saint Louis, MO 63101, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MAGiC Sweep EP Mapping Catheter Cable, Electrode Catheter, Electrode recording, or probe, electrode recording Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DRF Catheter, Electrode Recording, Or Probe, Electrode Recording Cardiovascular Class 2 870.1220 2026-04-28
IKD Cable, Electrode Physical Medicine Class 2 890.1175 2025-02-21
DRF Catheter, Electrode Recording, Or Probe, Electrode Recording Cardiovascular Class 2 870.1220 2025-02-21
OAE Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation Unknown Class 3 N/A 2025-02-21

Official Correspondent

Angela McKnight

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Stereotaxis
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3003084417 STEREOTAXIS, INC. Saint Louis, MO, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K881966 C.R. Bard, Inc. ELECTROPHYSIOLOGY ELECTRODE CATH. W/SILVER/SILVER 1988-10-04
K192037 ABBOTT MEDICAL Advisor VL Circular Mapping Catheter, Sensor Enabled 2019-09-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005402529. Last updated year: 2026. Please use registration number 3005402529 when referencing this establishment in official correspondence.
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