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CORE-RESISTANT HUBER INFUSION SET WITH Y-SITE

Page Type
Cleared 510(K)
510(k) Number
K950597
510(k) Type
Traditional
Applicant
DISTRONIC STERILE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/1995
Days to Decision
167 days
Submission Type
Summary

CORE-RESISTANT HUBER INFUSION SET WITH Y-SITE

Page Type
Cleared 510(K)
510(k) Number
K950597
510(k) Type
Traditional
Applicant
DISTRONIC STERILE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/1995
Days to Decision
167 days
Submission Type
Summary