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.

Siegen Corp.

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K871964 SIEGEN NEUROSCOPE SEEG FOR EVOKED RESPONSE STIMU.GWF1987-10-01 View
510(k) K861884 NEUROSCOPE SEEGGWO1986-10-14 View
510(k) K862430 SIEGEN HEADPHONESGWJ1986-09-26 View
510(k) K844616 SIEGEN VISUAL STIMULATORGWE1985-02-14 View
510(k) K844646 SIEGEN SURFACE ELECTRODESGXY1984-12-11 View
510(k) K843464 SIEGEN NEUROSCOPEGWF1984-11-20 View
↑