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FDA 510(k), K884832, PERCUSSIONAIRE RESPIRATORS (MULTIPLE)
FDA 510(k), K884832, PERCUSSIONAIRE RESPIRATORS (MULTIPLE)
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510(K) Number: K884832
Device Name: PERCUSSIONAIRE RESPIRATORS (MULTIPLE)
Manufacturer: BIRD, MD
Device Classification Name: Ventilator, Continuous, Facility Use
Regulation Number: CBK
Classification Product Code: KXA
Date Received: 11/18/1988
Decision Date: 09/14/1989
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
Device Name: PERCUSSIONAIRE RESPIRATORS (MULTIPLE)
Manufacturer: BIRD, MD
Device Classification Name: Ventilator, Continuous, Facility Use
Regulation Number: CBK
Classification Product Code: KXA
Date Received: 11/18/1988
Decision Date: 09/14/1989
Decision: Substantially Equivalent (SESE)
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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