
Konigsberg Instruments, Inc.
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MOTILITY PROBE MODEL NUMBERS P31 THRU P38, P40 THRU P43 AND P50 is an FDA 510(k)-cleared medical device (K980980) manufactured by Konigsberg Instruments, 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 June 14, 1998. Regulation: 8.