CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM
FDA 510(k) clearance K953314 · decided 1995-07-28
Clearance details
- K-number
- K953314
- Device name
- CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM
- Applicant
- Conceptus, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1995-07-12
- Decision date
- 1995-07-28
- Days to decision
- 16 days
- Clearance type
- Traditional
- Product code
- MOV
- Device class
- 2
- Regulation number
- 884.4530
- Medical specialty
- Obstetrics/Gynecology
- Advisory committee
- Obstetrics/Gynecology
- Location
- San Carlos, CA, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Conceptus
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| 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 |
Recalls involving this device
No recalls on record reference this clearance.