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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Set, Administration, Intravascular
510(k) Number K882798
Device Name MULTIFLO ADAPTER
Applicant
Deseret Medical, Inc.
9450 S. State St.
Sandy,  UT  84070
Applicant Contact CHARLES J WELLE
Correspondent
Deseret Medical, Inc.
9450 S. State St.
Sandy,  UT  84070
Correspondent Contact CHARLES J WELLE
Regulation Number880.5440
Classification Product Code
FPA  
Date Received07/06/1988
Decision Date 07/18/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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