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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K230130

Micromate™ Navi+ · Isys Medizintechnik GmbH · decided 2023-10-10 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Micromate Navi+iONEiSYS Medizintechnik GmbHJAK09010279001548