HYSTEROSCOPIC MYOMA SCREW
FDA 510(k) clearance K915412 · decided 1992-05-18
Clearance details
- K-number
- K915412
- Device name
- HYSTEROSCOPIC MYOMA SCREW
- Applicant
- Cook Urological, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1991-12-02
- Decision date
- 1992-05-18
- Days to decision
- 168 days
- Clearance type
- Traditional
- Product code
- HHO
- Device class
- 2
- Regulation number
- 884.4530
- Medical specialty
- Obstetrics/Gynecology
- Advisory committee
- Obstetrics/Gynecology
- Location
- Spencer, IN, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| LAPAROCOPIC MYOMA SCREW (K915388) | Cook Urological, Inc. | 1992-05-18 |
Recalls involving this device
No recalls on record reference this clearance.