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Verimed Holdings, Inc.

FDA 510(k) & PMA Approved Devices — 12 products

Total Devices12
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K981277 PERIFORMHIR1998-11-20 View
510(k) K954127 BIOFEEDBACK DEVICEHCC1995-11-14 View
510(k) K951969 MYOEXORCISER II FUALHCC1995-06-14 View
510(k) K930670 PHYACTION 787IPF1993-07-02 View
510(k) K922550 ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM)KQX1992-12-10 View
510(k) K913912 VERIMED PERINEOMETERHIR1992-06-16 View
510(k) K893220 VERIMED MYOEXORCISER VERISTIMIPF1990-03-07 View
510(k) K892649 VERIMED MYOEXORCISER III (MYO III)HCC1989-12-13 View
510(k) K874212 VERIMED MYO/PREMSIPF1988-08-08 View
510(k) K854193 ELECTRO-MYOGRAPHIC PERINEOMETERHIR1986-06-09 View
510(k) K852963 MYO-ACTUATORHCC1986-01-21 View
510(k) K832714 VERIMED MYOEXORCISERHCC1983-10-28 View
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