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.

Epitek, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K080780 ANCHORAGE SCOPE, MODEL 000003FBO2008-07-30 View
510(k) K073507 ANCHORAGE ACCESS KITODC2008-03-05 View
510(k) K073096 ANCHORAGE CLOSURE DEVICEGAT2008-02-07 View
↑