MOV
5 FDA 510(k) clearances · Product code
851 daysmedian time to decision
911 days90th percentile
5clearances measured
FDA profile
- Official device name
- Catheters, Salpingography
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 884.4530
- Medical specialty
- Obstetrics/Gynecology
- Flags
- Third-party review eligible
- Adverse events (MAUDE)
- 2002: 2
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| Modified Novy Cornual Cannulation Set (K180552) | Cook Incorporated | 2018-07-12 |
| ECHOMARK INTRAUTERINE GUIDING CATHETER (K932436) | Echocath, Inc. | 1995-11-16 |
| OVAMED INTRAUTERINE ACCESS CATHETER (K931534) | Ovamed Corp. | 1995-07-28 |
| NOVY CORNUAL CANNULATION SET (K931476) | Cook Ob/Gyn | 1995-07-28 |
| CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM (K953314) | Conceptus, Inc. | 1995-07-28 |
Track MOV automatically
Every clearance here is in the API, with alerts when new ones post.