FDA 510(k), K813639, SERIES 400 DISPOSABLE TEMPERATURE PROBE

FDA 510(k), K813639, SERIES 400 DISPOSABLE TEMPERATURE PROBE

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510(K) Number: K813639
Device Name: SERIES 400 DISPOSABLE TEMPERATURE PROBE
Manufacturer:
Device Classification Name: Thermometer, Electronic, Clinical
Regulation Number: FLL
Classification Product Code: KXA
Date Received: 12/31/1981
Decision Date: 01/22/1982
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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