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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Set, I.V. Fluid Transfer
510(k) Number K935274
Device Name DIPRIVAN LUER CONNECTOR
Applicant
Ohmeda Medical
2007 Pan Am Cir.
Tampa,  FL  33702
Applicant Contact RACHEL J SWATRIDGE
Correspondent
Ohmeda Medical
2007 Pan Am Cir.
Tampa,  FL  33702
Correspondent Contact RACHEL J SWATRIDGE
Regulation Number880.5440
Classification Product Code
LHI  
Date Received11/03/1993
Decision Date 03/15/1994
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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