Anyfusion, FDA registration completed with STeP | |
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The Safe Technologies Program (STeP) allows fast
track FDA 510K certification and pre-certification sales approval by quickly
reviewing medical devices that have significantly improved safety compared to
existing products in a timely manner. Anyfusion, a cylinder drug injection
pump, was filed with the FDA on August 26th as STeP Regardless of whether STeP is decided or not, we
will further develop Anyfusion to contribute to patients and medical staff with
safer equipment. Thank you for the hard work of Emergo consultant and related
parties during the preparation. Thank you. |
Next | An exclusive supply contract with Kuwait company for Anyfusion ACPi System |
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Prev | STeP Consulting Agreement for Fast Certification of Anyfusion FDA with UL(Emergo, USA) |