HDJ
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Scissors, Umbilical
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 884.4520
- Medical specialty
- Obstetrics/Gynecology
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| Record | Firm | Date | Builder |
|---|---|---|---|
| UMBILICAL SCISSORS (K890389) | Kinetic Medical Products | 1989-02-13 | + Add |
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Every clearance here is in the API, with alerts when new ones post.