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Neurologica Corporation

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K250928 OmniTom Elite with PCDJAK2025-09-08 View
510(k) K233767 OmniTom EliteJAK2024-06-10 View
510(k) K213649 BodyTom 64JAK2022-04-29 View
510(k) K171183 OmniTomJAK2017-08-18 View
510(k) K102677 BODYTOM NL 4000JAK2011-03-24 View
510(k) K090811 INSPIRA HD, MODEL: NL1000KPS2009-08-27 View
510(k) K051765 CERETOM, MODEL NL3000JAK2005-07-14 View
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