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

Clearance record K121253

MERIDIAN CRANIAL PERFORATOR · Adeor Medical Technologies GmbH · decided 2012-07-17 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Meridian Perforatoralphaadeor Medical AGHBFEADEPER1114SG1
Meridian Perforatoralphaadeor Medical AGHBFEADEPER1114S1
Meridian PerforatorClassicadeor Medical AGHBFEADEPERC69S1
Meridian PerforatorClassicadeor Medical AGHBFEADEPERC811S1
Meridian Perforatoralphaadeor Medical AGHBFEADEPER1114SP1
Meridian Perforatoralphaadeor Medical AGHBFEADEPER711SP1
Meridian PerforatorClassicadeor Medical AGHBFEADEPERC1114S1
Meridian Perforatoralphaadeor Medical AGHBFEADEPER711S1