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

Clearance record K211817

Anterion · Heidelberg Engineering GmbH · decided 2021-11-05 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
ANTERIONSoftware with HEYEX 2 V1.2.3Heidelberg Engineering GmbHOBO04059237000754
ANTERION88036Heidelberg Engineering GmbHOBO04059237000877
ANTERION88036Heidelberg Engineering GmbHOBO04059237000617