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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name condenser, heat and moisture (artificial nose)
510(k) Number K904338
Device Name ICOR HCH 4, ICOR HCH 7
Applicant
ICOR AB
ULVSUNDAVAGEN 178 B
BROMMA,  SE 161 30
Applicant Contact ANDRAS GEDEON
Correspondent
ICOR AB
ULVSUNDAVAGEN 178 B
BROMMA,  SE 161 30
Correspondent Contact ANDRAS GEDEON
Regulation Number868.5375
Classification Product Code
BYD  
Date Received09/20/1990
Decision Date 12/04/1990
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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