FDA 510(k), K123361, ESOTEST ESOPHAGEAL TEMPERATURE PROBE AND TEMPERATURE MONITORING SYSTEM
FDA 510(k), K123361, ESOTEST ESOPHAGEAL TEMPERATURE PROBE AND TEMPERATURE MONITORING SYSTEM
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510(K) Number: K123361
Device Name: ESOTEST ESOPHAGEAL TEMPERATURE PROBE AND TEMPERATURE MONITORING SYSTEM
Manufacturer:
Device Classification Name: Thermometer, Electronic, Clinical
Regulation Number: 880.2910
Classification Product Code: FLL
Date Received: 10/31/2012
Decision Date: 02/27/2013
Regulation Medical Specialty: General Hospital
Device Name: ESOTEST ESOPHAGEAL TEMPERATURE PROBE AND TEMPERATURE MONITORING SYSTEM
Manufacturer:
Device Classification Name: Thermometer, Electronic, Clinical
Regulation Number: 880.2910
Classification Product Code: FLL
Date Received: 10/31/2012
Decision Date: 02/27/2013
Regulation Medical Specialty: General Hospital