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.

Charlton Assoc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K951136 BIONIKE A/Q PREGNANCY TESTJHI1995-04-20 View
510(k) K941771 BODYWISE PREGNANCEY TESTLCX1994-07-06 View
↑