FDA 510(k), K030611, MODIFICATION TO SUZANNE PORTABLE POLYSOMNOGRAPH SYSTEM

FDA 510(k), K030611, MODIFICATION TO SUZANNE PORTABLE POLYSOMNOGRAPH SYSTEM

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510(K) Number: K030611
Device Name: MODIFICATION TO SUZANNE PORTABLE POLYSOMNOGRAPH SYSTEM
Manufacturer:
Device Classification Name: Ventilatory Effort Recorder
Regulation Number: 868.2375
Classification Product Code: MNR
Date Received: 02/26/2003
Decision Date: 03/24/2003
Regulation Medical Specialty: Anesthesiology
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