FDA 510(k), K910091, ULTRALITE PANELITE

FDA 510(k), K910091, ULTRALITE PANELITE

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510(K) Number: K910091
Device Name: ULTRALITE PANELITE
Manufacturer: ULTRALITE
Device Classification Name: lamp, infrared, non heating
Regulation Number: 890.5500
Classification Product Code: IOB
Date Received: 01/09/1991
Decision Date: 05/30/1991
Regulation Medical Specialty: Physical Medicine
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