KZH
- Product code
- KZH
- Device name
- Introducer, Syringe Needle
- Device class
- Class 2
- 21 CFR
- 21 CFR 880.6920
- Medical specialty
- General Hospital
- Marketing pathway
- 510(K)
- 510(k) clearances (last 3 years)
- 1
- Summaries archived here
- 1 (direct download)
- 510(k) clearances (all years, FDA)
- 47 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K243232 | 2024-12-02 | Synthon Hispania S.L. | GripMate |
Official FDA classification page: KZH
Classification and pathway per current FDA publications. Data from openFDA (CC0).