FDA Updates Guidance on Third-Party 510(k) Review Program
The FDA issued updated guidance on the 510(k) Third Party Review Program and EUA Review, clarifying expectations, processes, and criteria.
The FDA issued updated guidance on the 510(k) Third Party Review Program and EUA Review, clarifying expectations, processes, and criteria.
The new advisory highlights the importance of how surgical instruments and other critical devices are reprocessed and reused every day in healthcare.
The Medicare Coverage of Innovative Technologies Pathway could help promote product innovation by preventing costly delays in coverage.
The FDA issued updated guidance on the 510(k) Third Party Review Program and EUA Review, clarifying expectations, processes, and criteria.