
Hollister, Inc.
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VAGINAL 2 ELECTRODE STIMULATION/EMG PROBE-SMALL is an FDA 510(k)-cleared medical device (K970602) manufactured by Hollister, 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 April 14, 1997. Regulation: 8.