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U.S. Department of Health and Human Services

Product Classification

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Device computer, diagnostic, pre-programmed, single-function
Regulation Medical Specialty Cardiovascular
Review Panel Cardiovascular
Product CodeDXG
Premarket Review Cardiovascular Devices (OHT2)
Cardiac Electrophysiology, Diagnostics, and Monitoring Devices (DHT2A)
Submission Type 510(k)
Regulation Number 870.1435
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Summary Malfunction
Reporting
Eligible
Implanted Device? No
Life-Sustain/Support Device? No
Third Party Review
Accredited Persons
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