Verimed Holdings, Inc.
Verimed Holdings, Inc. holds FDA 510(k) medical device clearances, first cleared 1983, most recent 1998.
Top product codes for Verimed Holdings, Inc.
Recent clearances by Verimed Holdings, Inc.
- K981277 — PERIFORM
- K954127 — BIOFEEDBACK DEVICE
- K951969 — MYOEXORCISER II FUAL
- K930670 — PHYACTION 787
- K922550 — ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM)
- K913912 — VERIMED PERINEOMETER
- K893220 — VERIMED MYOEXORCISER VERISTIM
- K892649 — VERIMED MYOEXORCISER III (MYO III)
- K874212 — VERIMED MYO/PREMS
- K854193 — ELECTRO-MYOGRAPHIC PERINEOMETER
- K852963 — MYO-ACTUATOR
- K832714 — VERIMED MYOEXORCISER
Data sourced from openFDA. This site is unofficial and independent of the FDA.