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U.S. Department of Health and Human Services

Product Classification

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Device thermometer, electronic, clinical
Regulation Description Clinical electronic thermometer.
Regulation Medical Specialty General Hospital
Review Panel General Hospital
Product CodeFLL
Premarket Review Office of Gastrorenal, ObGyn, General Hospital, and Urology Devices (OHT3)
Drug Delivery and General Hospital Devices, and Human Factors (DHT3C)
Submission Type 510(k)
Regulation Number 880.2910
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
Recognized Consensus Standards
Guidance Document
Third Party Review
Accredited Persons
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