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Verimed Holdings, Inc.

12 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
PERIFORM (K981277)Verimed Holdings, Inc.1998-11-20
BIOFEEDBACK DEVICE (K954127)Verimed Holdings, Inc.1995-11-14
MYOEXORCISER II FUAL (K951969)Verimed Holdings, Inc.1995-06-14
PHYACTION 787 (K930670)Verimed Holdings, Inc.1993-07-02
ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM) (K922550)Verimed Holdings, Inc.1992-12-10
VERIMED PERINEOMETER (K913912)Verimed Holdings, Inc.1992-06-16
VERIMED MYOEXORCISER VERISTIM (K893220)Verimed Holdings, Inc.1990-03-07
VERIMED MYOEXORCISER III (MYO III) (K892649)Verimed Holdings, Inc.1989-12-13
VERIMED MYO/PREMS (K874212)Verimed Holdings, Inc.1988-08-08
ELECTRO-MYOGRAPHIC PERINEOMETER (K854193)Verimed Holdings, Inc.1986-06-09
MYO-ACTUATOR (K852963)Verimed Holdings, Inc.1986-01-21
VERIMED MYOEXORCISER (K832714)Verimed Holdings, Inc.1983-10-28

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