510(k) K840656

ENTERNAL Y EXTENSION SET RECORDER by Corpak Medsystems — Product Code KNT

K840656 is an FDA 510(k) premarket notification submitted by Corpak Medsystems for the device "ENTERNAL Y EXTENSION SET RECORDER". The FDA issued a decision of Substantially Equivalent on April 4, 1984. The device falls under product code KNT (Tubes, Gastrointestinal (And Accessories)), a Class II device regulated under 21 CFR 876.5980. Corpak Medsystems has at least 10 other 510(k) clearances on record.