FDA 510(k), K811742, HEMOTHERM MODEL 400

FDA 510(k), K811742, HEMOTHERM MODEL 400

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510(K) Number: K811742
Device Name: HEMOTHERM MODEL 400
Manufacturer:
Device Classification Name: System, Thermal Regulating
Regulation Number: DWJ
Classification Product Code: KXA
Date Received: 06/19/1981
Decision Date: 08/13/1981
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
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