Dyansys, Inc.
Dyansys, Inc. holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2022.
Top product codes for Dyansys, Inc.
Recent clearances by Dyansys, Inc.
- K221425 — Primary Relief
- K221231 — Drug Relief v1
- K220397 — ANSiStim-PP
- K213188 — Primary Relief
- K212859 — First Relief
- K211971 — Drug Relief v1
- K202940 — First Relief v1
- K173861 — Drug Relief
- K170391 — ANSiStim-PP
- K141168 — ANSISTIM
- K091397 — ECSCOPE 200
- K091358 — ECSCOPE 100
- K080036 — PORTABLE ECSCOPE 12I
- K071168 — THE PORTABLE ANSISCOPE
Data sourced from openFDA. This site is unofficial and independent of the FDA.