Zyto Technologies, Inc.
Zyto Technologies, Inc. holds FDA 510(k) medical device clearance, cleared in 2011, with 2 FDA device recalls on record.
Top product codes for Zyto Technologies, Inc.
FDA recalls by Zyto Technologies, Inc.
- Z-2120-2016 — The ZYTO Tower is the input device to program the software with various virtual items.
- Z-2121-2016 — The ZYTO Select and ZYTO Elite software programs are used to rank pairs of galvanic skin response measurements from most coherent (the second scan is closest in time measurement to the baseline original scan) to least coherent (further away from the baseline).
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Zyto Technologies, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.