LTC
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Hyaline Membrane Disease Assay
- Device class
- Class III (high risk)
- Medical specialty
- Unknown
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| Record | Firm | Date | Builder |
|---|---|---|---|
| WHITESIDE ACRYLIC CEMENT SPACER SLEEVE (K844637) | Dow Corning Corp. Healthcare Industries Materials | 1985-06-19 | + Add |
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Every clearance here is in the API, with alerts when new ones post.