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FDA 510(k), K905236, IPV PERCUSSIONATOR FAMILY & RELATED ACCESSORIES
FDA 510(k), K905236, IPV PERCUSSIONATOR FAMILY & RELATED ACCESSORIES
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510(K) Number: K905236
Device Name: IPV PERCUSSIONATOR FAMILY & RELATED ACCESSORIES
Manufacturer: PERCUSSIONAIRE CORP.
Device Classification Name: device, positive pressure breathing, intermittent
Regulation Number: 868.5905
Classification Product Code: NHJ
Date Received: 11/07/1990
Decision Date: 04/18/1991
Regulation Medical Specialty: Anesthesiology
Device Name: IPV PERCUSSIONATOR FAMILY & RELATED ACCESSORIES
Manufacturer: PERCUSSIONAIRE CORP.
Device Classification Name: device, positive pressure breathing, intermittent
Regulation Number: 868.5905
Classification Product Code: NHJ
Date Received: 11/07/1990
Decision Date: 04/18/1991
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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