Verimed Holdings, Inc.
FDA 510(k) medical device clearances.
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.