Product code MOV— Obstetrics/Gynecology

FDA has cleared 5 devices under product code MOV between 1995 and 2018, filed by 5 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

• 20181 clearance
• 19954 clearances

• Ovamed Corp.1 clearance
• Echocath, Inc.1 clearance
• Cook Ob/Gyn1 clearance
• Cook Incorporated1 clearance
• Conceptus, Inc.1 clearance

• K180552 — Modified Novy Cornual Cannulation SetCook Incorporated·2018-07-12
• K932436 — ECHOMARK INTRAUTERINE GUIDING CATHETEREchocath, Inc.·1995-11-16
• K931476 — NOVY CORNUAL CANNULATION SETCook Ob/Gyn·1995-07-28
• K931534 — OVAMED INTRAUTERINE ACCESS CATHETEROvamed Corp.·1995-07-28
• K953314 — CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEMConceptus, Inc.·1995-07-28