
Northgate Technologies, Inc.
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1.9 FRENCH LITHOTRIPTER ELECTRODE, MODIFICATION is an FDA 510(k)-cleared medical device (K914514) manufactured by Northgate Technologies, Inc.. 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 January 5, 1992. Regulation: 8.