510(k) K131157

RANFAC BONE MARROW ASPIRATION NEEDLE by Ranfac, Corp. — Product Code KNW

K131157 is an FDA 510(k) premarket notification submitted by Ranfac, Corp. for the device "RANFAC BONE MARROW ASPIRATION NEEDLE". The FDA issued a decision of Substantially Equivalent on October 22, 2013. The device falls under product code KNW (Instrument, Biopsy), a Class II device regulated under 21 CFR 876.1075. Ranfac, Corp. has at least 10 other 510(k) clearances on record.