FDA device listing

Blazer II HTD Temperature Ablation Catheter,Blazer II Temperature Ablation Catheter,Blazer Prime HTD Temperature…

FDA device listing 1923360514 · Boston Scientific Corporation

Key facts

Proprietary names Blazer II HTD Temperature Ablation Catheter,Blazer II Temperature Ablation Catheter,Blazer Prime HTD Temperature Ablation Catheter,Blazer Solid-Tip Ablation Catheter Cable, Sterile Cable,Cable, IntellaNav Ablation Catheter,Electrophysiology Cable Sterile Cable,INTELLAGEN Catheter Adapter Cable 0.3 Meter,INTELLAGEN ECG Connection Cable 3 Meter,INTELLAGEN Foot Pedal,INTELLAGEN Foot Pedal Extension…
Owner/operator Boston Scientific Corporation
Owner/operator number 9912058
Premarket submissions P920047
Product codes LPB
Device names LPB - Cardiac Ablation Percutaneous Catheter
Device class Class III
Classification regulations (21 CFR) ORCA1.LPB
Review panels Cardiovascular
Registered establishments Boston Scientific Corporation, BOSTON SCIENTIFIC CORPORATION, Boston Scientific Limited
Establishment registrations 2124215, 9681260, 1000121056, 3004859241, 3007695959
FEI numbers 2124215, 1000121056, 3002806565, 3004859241, 3007695959
Establishment operations Complaint File Establishment, Manufacturer, Specification Developer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • 10–99 UDI devices (GUDID) under the same submission
  • 1–9 Device listings citing the same submission
  • Yes Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

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