510(k) K982085

MEDICAL DEVICE TECHNOLOGIES, INC. TRU-CORE DISPOSALE SEMI-AUTOMATIC BIOPDY INSTRUMENT by Medical Device Technologies, Inc. — Product Code KNW

K982085 is an FDA 510(k) premarket notification submitted by Medical Device Technologies, Inc. for the device "MEDICAL DEVICE TECHNOLOGIES, INC. TRU-CORE DISPOSALE SEMI-AUTOMATIC BIOPDY INSTRUMENT". The FDA issued a decision of Substantially Equivalent on July 17, 1998. The device falls under product code KNW (Instrument, Biopsy), a Class II device regulated under 21 CFR 876.1075. Medical Device Technologies, Inc. has at least 10 other 510(k) clearances on record.