
Pentax Precision Instrument Corp.
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PENTAX FG-34JA GASTROFIBERSCOPE is an FDA 510(k)-cleared medical device (K832007) manufactured by Pentax Precision Instrument Corp.. 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 August 10, 1983. Regulation: 8.