Precision S 4K Sinuscope

Precision S 4K Sinuscope is an FDA 510(k)-cleared medical device (K253602) manufactured by Stryker Endoscopy. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 3, 2026. Regulation: 8.