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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name ventilator, continuous, facility use
510(k) Number K900313
Device Name PERCUSSIONAIRE(R) VDR-3 IMV PERCUS/RESPIR 1250 MIN
Applicant
PERCUSSIONAIRE CORP.
BIRD AIRLODGE, GLENGARY BAY
P.O. BOX 817
SANDPOINT,  ID  83864
Applicant Contact BIRD, MD
Correspondent
PERCUSSIONAIRE CORP.
BIRD AIRLODGE, GLENGARY BAY
P.O. BOX 817
SANDPOINT,  ID  83864
Correspondent Contact BIRD, MD
Regulation Number868.5895
Classification Product Code
CBK  
Date Received01/22/1990
Decision Date 10/26/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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