
Applied Medical Technologies
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P.R.G. GUIDEWIRE PLACEMENT SYSTEM is an FDA 510(k)-cleared medical device (K903036) manufactured by Applied Medical Technologies. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 18, 1990. Regulation: 8.