
Richard-Allan Medical
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REFLEX(R) EHS (ENDOSCOPIC HERNIA STAPLER) is an FDA 510(k)-cleared medical device (K933901) manufactured by Richard-Allan Medical. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 18, 1993. Regulation: 8.

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