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

Clearance record K213932

A-dec 300, A-dec 500 · A-Dec, Inc. · decided 2022-03-02 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
A-dec335proA-DEC, INC.EIA10194665005917
A-dec334proA-DEC, INC.EIA10194665005870
A-dec541proA-DEC, INC.EIA10194665005412
A-dec532proA-DEC, INC.EIA10194665005320
A-dec333proA-DEC, INC.EIA10194665005863
A-dec551staA-DEC, INC.EIA10194665005429
A-dec341spA-DEC, INC.EIA10194665006730
A-dec341fltA-DEC, INC.EIA10194665005993
A-dec342proA-DEC, INC.EIA10194665005900
A-dec341proA-DEC, INC.EIA10194665005986
A-dec533proA-DEC, INC.EIA10194665005405
A-dec545staA-DEC, INC.EIA10194665005436
A-dec343proA-DEC, INC.EIA10194665007300
A-dec332fltA-DEC, INC.EIA10194665005399
A-dec336proA-DEC, INC.EIA10194665005894
A-dec332proA-DEC, INC.EIA10194665005856