FDA 510(k), K033820, MICROLIFE DIGITAL INFRARED FOREHEAD THERMOMETER, MODEL FR1DM1
FDA 510(k), K033820, MICROLIFE DIGITAL INFRARED FOREHEAD THERMOMETER, MODEL FR1DM1
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510(K) Number: K033820
Device Name: MICROLIFE DIGITAL INFRARED FOREHEAD THERMOMETER, MODEL FR1DM1
Manufacturer:
Device Classification Name: Thermometer, Electronic, Clinical
Regulation Number: 880.2910
Classification Product Code: FLL
Date Received: 12/09/2003
Decision Date: 02/23/2004
Regulation Medical Specialty: General Hospital
Device Name: MICROLIFE DIGITAL INFRARED FOREHEAD THERMOMETER, MODEL FR1DM1
Manufacturer:
Device Classification Name: Thermometer, Electronic, Clinical
Regulation Number: 880.2910
Classification Product Code: FLL
Date Received: 12/09/2003
Decision Date: 02/23/2004
Regulation Medical Specialty: General Hospital