
S.A.I.E.P. S.R.L.
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FILM PROCESSOR, MODEL LIFE RAY PRO 1000 is an FDA 510(k)-cleared medical device (K023801) manufactured by S.A.I.E.P. S.R.L.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 11, 2003. Regulation: 8.

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