510(k) K871691

MODIFIED MULTI-LUMEN NASOGASTRIC TUBE by Bissell Medical Products, Inc. — Product Code KNT

K871691 is an FDA 510(k) premarket notification submitted by Bissell Medical Products, Inc. for the device "MODIFIED MULTI-LUMEN NASOGASTRIC TUBE". The FDA issued a decision of Substantially Equivalent on August 10, 1987. The device falls under product code KNT (Tubes, Gastrointestinal (And Accessories)), a Class II device regulated under 21 CFR 876.5980. Bissell Medical Products, Inc. has at least 5 other 510(k) clearances on record.