FDA 510(k), K904834, INTAVENT LARYNGEAL MASK

FDA 510(k), K904834, INTAVENT LARYNGEAL MASK

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510(K) Number: K904834
Device Name: INTAVENT LARYNGEAL MASK
Manufacturer: INTAVENT INTL. S.A.
Device Classification Name: Airway, Oropharyngeal, Anesthesiology
Regulation Number: 868.5110
Classification Product Code: CAE
Date Received: 10/24/1990
Decision Date: 07/26/1991
Regulation Medical Specialty: Anesthesiology
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