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U.S. Department of Health and Human Services

Product Classification

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Device catheter, intravascular, diagnostic
Regulation Description Diagnostic intravascular catheter.
Regulation Medical Specialty Cardiovascular
Review Panel Cardiovascular
Product CodeDQO
Premarket Review Cardiovascular Devices (OHT2)
Cardiac Electrophysiology, Diagnostics, and Monitoring Devices (DHT2A)
Submission Type 510(k)
Regulation Number 870.1200
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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