Product code KYW
- Device name
- Container, Liquid Medication, Graduated
- Medical specialty
- General Hospital
- Device class
- 1
- Regulation number
- 880.6430
- Review panel
- HO
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- Y
- Third party review
- N
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset
Related 510(k) Records#
Related GUDID Devices#
| Primary DI | Brand | Company | Published |
|---|---|---|---|
| 00724995252830 | V. Mueller | Steris Corporation | 2026-08-21 |
| 00724995252847 | V. Mueller | Steris Corporation | 2026-08-21 |
| 00724995252892 | V. Mueller | Steris Corporation | 2026-08-21 |
| 00724995252908 | V. Mueller | Steris Corporation | 2026-08-21 |
| 00724995252915 | V. Mueller | Steris Corporation | 2026-08-21 |
| 00724995252922 | V. Mueller | Steris Corporation | 2026-08-21 |
| 00724995252823 | V. Mueller | Steris Corporation | 2026-08-21 |
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