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.

Pro-Tronics, Inc.

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

Total Devices5
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K950971 MOBIL C-ARM, REGURBISHED, VARIOUS MODELSJAA1995-04-11 View
510(k) K944442 GENERAL ELECTRIC AMX 110, AMX II AND AMX 3IZL1995-03-14 View
510(k) K902610 GENERAL ELECTRIC AMX 3IZL1990-07-02 View
510(k) K891143 GENERAL ELECTRIC AMX 110IZL1989-05-03 View
510(k) K891142 GENERAL ELECTRIC AMX IIIZL1989-05-01 View
↑