
Pulse Biosciences, Inc.
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CellFX Percutaneous Electrode System (SYS3000) is an FDA 510(k)-cleared medical device (K233705) manufactured by Pulse Biosciences, 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 March 7, 2024. Regulation: 8.