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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