HWI
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Corkscrew
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 888.4540
- Medical specialty
- Orthopedic
- Adverse events (MAUDE)
- 1999: 1
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
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| Record | Firm | Date | Builder |
|---|---|---|---|
| PHARMASEAL STERILE UMBILICAL CORD CLAMP (K875166) | Baxter Healthcare Corp | 1988-03-02 | + Add |
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