medical device engineering: development, design control, 510k submissions, pma submissions, risk analysis, validation, verification, design, prototyping, submissions, premarket approval, pma, premarket notification, 510(k), 510k, and risk analysis are services toltec provides for fda regulated devices.
The http-equiv attribute provides an HTTP header for the information/value of the content attribute. The http-equiv attribute can be used to simulate an HTTP response header.