KYW
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Container, Liquid Medication, Graduated
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 880.6430
- Medical specialty
- General Hospital
- Flags
- GMP exempt
- Adverse events (MAUDE)
- 2019: 38 · 2020: 24 · 2021: 15 · 2022: 35 · 2023: 19 · 2026: 17
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| PHARMACY ADDITIVE SYRINGE SET (K800213) | Cutter Laboratories, Inc. | 1980-02-26 |
| MEDICINE CUP (K791345) | General Clinical Plastics Corp. | 1979-08-03 |
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