510(k) K932072

JARIT SURGICAL INSTRUMENTS by Medical Device Inspection Co., Inc. — Product Code HET

K932072 is an FDA 510(k) premarket notification submitted by Medical Device Inspection Co., Inc. for the device "JARIT SURGICAL INSTRUMENTS". The FDA issued a decision of Substantially Equivalent on January 11, 1994. The device falls under product code HET (Laparoscope, Gynecologic (And Accessories)), a Class II device regulated under 21 CFR 884.1720. Medical Device Inspection Co., Inc. has at least 10 other 510(k) clearances on record.