Recognized a 510(k)/PMA number — showing its clearance record and devices.
Clearance record K190744
ENDOEYE HD II (WA50040A, WA50042A, WA50050A, WA50052A) · Olympus Winter & Ibe GmbH · decided 2019-08-29 (SESE)
FDA 510(k) database ↗Summary PDF ↗
No GUDID device is registered under this submission yet — registration typically lags clearance by months.
Devices
No matching devices.
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