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SMARTSITE VENTED VIAL ACCESS DEVICE, MODEL TBD

Page Type
Cleared 510(K)
510(k) Number
K052790
510(k) Type
Traditional
Applicant
CARDINAL HEALTH, ALARIS PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2005
Days to Decision
81 days
Submission Type
Summary

SMARTSITE VENTED VIAL ACCESS DEVICE, MODEL TBD

Page Type
Cleared 510(K)
510(k) Number
K052790
510(k) Type
Traditional
Applicant
CARDINAL HEALTH, ALARIS PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2005
Days to Decision
81 days
Submission Type
Summary