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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 K842122
Device Name 4A
Applicant
LIFE PRODUCTS, INC.
2545 CENTRAL AVE.
BOULDER,  CO  80301
Applicant Contact DOUGLAS BARNES
Correspondent
LIFE PRODUCTS, INC.
2545 CENTRAL AVE.
BOULDER,  CO  80301
Correspondent Contact DOUGLAS BARNES
Regulation Number868.5895
Classification Product Code
CBK  
Date Received05/29/1984
Decision Date 01/18/1985
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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