FDA 510(k) Applications Submitted by STERIPAK, LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K980829 03/04/1998 3ML STERI-NEB SALINE - 0.9% W/V SODIUM CHLORIDE INHALATION SOLUTION USP STERIPAK, LTD.
K972185 06/10/1997 20 ML NORMAL SALINE TOPICAL SOLUTION, 0.9% W/V SODIUM CHLORIDE STERIPAK, LTD.


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