510(k) K070475

MODIFICATON TO: GIVEN DIAGNOSTIC IMAGING SYSTEM by Given Imaging , Ltd. — Product Code NEZ

K070475 is an FDA 510(k) premarket notification submitted by Given Imaging , Ltd. for the device "MODIFICATON TO: GIVEN DIAGNOSTIC IMAGING SYSTEM". The FDA issued a decision of Substantially Equivalent on May 7, 2007. The device falls under product code NEZ (System, Imaging, Gastrointestinal, Wireless, Capsule), a Class II device regulated under 21 CFR 876.1300. Given Imaging , Ltd. has at least 10 other 510(k) clearances on record.