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LIFTLOC SAFETY INFUSION SET

Page Type
Cleared 510(K)
510(k) Number
K013394
510(k) Type
Traditional
Applicant
SPECIALIZED HEALTH PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2001
Days to Decision
24 days
Submission Type
Summary

LIFTLOC SAFETY INFUSION SET

Page Type
Cleared 510(K)
510(k) Number
K013394
510(k) Type
Traditional
Applicant
SPECIALIZED HEALTH PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2001
Days to Decision
24 days
Submission Type
Summary