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.

American Midwest

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K821895 AH-1 LIGHT-CURE DENTAL COMPOSITE RESTOREBF1982-07-16 View
510(k) K821715 AM-40 SYSTEMEFB1982-06-25 View
510(k) K820693 MIDWEST LIGHT WANDEBZ1982-04-09 View
510(k) K811979 ATT-1 DENTAL COMPOSITE RESTORATIVE SYSEBF1981-08-18 View
510(k) K800735 U-STYLE ADAPTEREGS1980-04-10 View
↑