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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 K003254
Device Name CORTEZ NEEDLE FREE IV CONNECTOR, MODEL MMD-001
Applicant
MISSION MEDICL DEVICES
3525 del mar heights rd. #430
san diego,  CA  92130
Contact donald v canal
Regulation Number880.5440
Classification Product Code
FPA  
Date Received10/17/2000
Decision Date 07/09/2001
Decision substantially equivalent (SE)
Classification Advisory Committee General Hospital
Review Advisory Committee General Hospital
summary summary
Type Traditional
Reviewed by Third Party No
Expedited Review No
Combination Product No
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