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FDA 510(k), K905235, VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS
FDA 510(k), K905235, VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS
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510(K) Number: K905235
Device Name: VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS
Manufacturer: PERCUSSIONAIRE CORP.
Device Classification Name: ventilator, continuous, facility use
Regulation Number: 868.5895
Classification Product Code: CBK
Date Received: 11/07/1990
Decision Date: 05/03/1991
Regulation Medical Specialty: Anesthesiology
Device Name: VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS
Manufacturer: PERCUSSIONAIRE CORP.
Device Classification Name: ventilator, continuous, facility use
Regulation Number: 868.5895
Classification Product Code: CBK
Date Received: 11/07/1990
Decision Date: 05/03/1991
Regulation Medical Specialty: Anesthesiology
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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