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FDA 510(k) Applications Submitted by DISTRONIC STERILE PRODUCTS, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K955732
12/19/1995
VENTED SOLUTION SET
DISTRONIC STERILE PRODUCTS, INC.
K954983
10/31/1995
EXTENSION SET WITH CHECK VALVE
DISTRONIC STERILE PRODUCTS, INC.
K954984
10/31/1995
MINIBORE STOPCOCK SET
DISTRONIC STERILE PRODUCTS, INC.
K955709
12/18/1995
WINGED & SUBCUTANEOUS INFUSION SETS
DISTRONIC STERILE PRODUCTS, INC.
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