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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stretcher, Wheeled
510(k) Number K933366
Device Name I.V. LINK
Applicant
Deville Laboratories, Inc.
9986 N. Newport Hwy.
Suite 165
Spokane,  WA  99218
Applicant Contact TRINA STARKEY
Correspondent
Deville Laboratories, Inc.
9986 N. Newport Hwy.
Suite 165
Spokane,  WA  99218
Correspondent Contact TRINA STARKEY
Regulation Number880.6910
Classification Product Code
FPO  
Date Received07/09/1993
Decision Date 01/10/1994
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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