510(k) K760183

OBTURATOR, DEFLECTING by V. Mueller O.V. Baxter Healthcare Corp. — Product Code FEC

K760183 is an FDA 510(k) premarket notification submitted by V. Mueller O.V. Baxter Healthcare Corp. for the device "OBTURATOR, DEFLECTING". The FDA issued a decision of Substantially Equivalent on December 2, 1976. The device falls under product code FEC (Obturator, For Endoscope), a Class II device regulated under 21 CFR 876.1500. V. Mueller O.V. Baxter Healthcare Corp. has at least 10 other 510(k) clearances on record.