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

Clearance record K180394

BrightMatter Plan 1.6.0 · Synaptive Medical, Inc. · decided 2018-03-09 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Modus Plan2.1Synaptive Medical IncLLZ00670082000511
Modus Plan2.0Synaptive Medical IncLLZ00670082000443
Modus Plan2.2Synaptive Medical IncLLZ00670082000610
BrightMatter Plan1.6Synaptive Medical IncLLZ00670082000412