510(k) K950898

BIOBOX WITH FUNNEL TOP (SMALL, MEDIUM, LARGE, AND X-LARGE) by Biosystems — Product Code MMK

K950898 is an FDA 510(k) premarket notification submitted by Biosystems for the device "BIOBOX WITH FUNNEL TOP (SMALL, MEDIUM, LARGE, AND X-LARGE)". The FDA issued a decision of Substantially Equivalent on August 24, 1995. The device falls under product code MMK (Container, Sharps), a Class II device regulated under 21 CFR 880.5570. Biosystems has at least 6 other 510(k) clearances on record.