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.

Hall Laboratories, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K881514 PRISTINE SPECIMEN TUBE AND INTRODUCER SYSTEMBSK1988-06-16 View
510(k) K874645 CLOSED WOUND DRAINAGE SYSTEMSGCY1987-12-02 View
↑