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U.S. Department of Health and Human Services

Product Classification

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Device catheter, recording, electrode, reprocessed
Regulation Description Electrode recording catheter or electrode recording probe.
Regulation Medical Specialty Cardiovascular
Review Panel Cardiovascular
Product CodeNLH
Premarket Review Office of Device Evaluation (ODE)
Division of Cardiovascular Devices (DCD)
Cardiac Electrophysiology Devices Branch (CEDB)
Submission Type 510(k)
Regulation Number 870.1220
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Third Party Review Not Third Party Eligible
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