510(k) K990906

FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER by Ferris Mfg. Corp. — Product Code KMF

K990906 is an FDA 510(k) premarket notification submitted by Ferris Mfg. Corp. for the device "FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER". The FDA issued a decision of SN on April 29, 1999. The device falls under product code KMF (Bandage, Liquid), a Class I device regulated under 21 CFR 880.5090. Ferris Mfg. Corp. has at least 10 other 510(k) clearances on record.