510(k) K960698

NON-CORING NEEDLE by Med Institute, Inc. — Product Code FMI

K960698 is an FDA 510(k) premarket notification submitted by Med Institute, Inc. for the device "NON-CORING NEEDLE". The FDA issued a decision of Substantially Equivalent on April 15, 1996. The device falls under product code FMI (Needle, Hypodermic, Single Lumen), a Class II device regulated under 21 CFR 880.5570. Med Institute, Inc. has at least 10 other 510(k) clearances on record.