
Roche Diabetes Care, Inc.
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Accu-Chek Safe-T-Pro Plus Lancing Device is an FDA 510(k)-cleared medical device (K220849) manufactured by Roche Diabetes Care, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 18, 2022. Regulation: 8.