UMBILICAL SCISSORS
FDA 510(k) clearance K890389 · decided 1989-02-13
Clearance details
- K-number
- K890389
- Device name
- UMBILICAL SCISSORS
- Applicant
- Kinetic Medical Products
- Decision
- Substantially Equivalent
- Date received
- 1989-01-23
- Decision date
- 1989-02-13
- Days to decision
- 21 days
- Clearance type
- Traditional
- Product code
- HDJ
- Device class
- 1
- Regulation number
- 884.4520
- Medical specialty
- Obstetrics/Gynecology
- Advisory committee
- Obstetrics/Gynecology
- Location
- Erie, PA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.