Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Steripak, Ltd.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K980829 3ML STERI-NEB SALINE - 0.9% W/V SODIUM CHLORIDE INHALATION SOLUTION USPCAF1998-06-02 View
510(k) K972185 20 ML NORMAL SALINE TOPICAL SOLUTION, 0.9% W/V SODIUM CHLORIDEFRO1998-03-05 View
↑