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FDA 510(k), K895486, BIRD (VDR) SINUSOIDAL PERCUSSIONATORS
FDA 510(k), K895486, BIRD (VDR) SINUSOIDAL PERCUSSIONATORS
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510(K) Number: K895486
Device Name: BIRD (VDR) SINUSOIDAL PERCUSSIONATORS
Manufacturer: FORREST M BIRD
Device Classification Name: Ventilator, Continuous, Facility Use
Regulation Number: CBK
Classification Product Code: KXA
Date Received: 09/11/1989
Decision Date: 10/13/1989
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
Device Name: BIRD (VDR) SINUSOIDAL PERCUSSIONATORS
Manufacturer: FORREST M BIRD
Device Classification Name: Ventilator, Continuous, Facility Use
Regulation Number: CBK
Classification Product Code: KXA
Date Received: 09/11/1989
Decision Date: 10/13/1989
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.
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