JEG
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Analyzer, Gas, Argon, Gaseous-Phase
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 868.1075
- Medical specialty
- Anesthesiology
- Flags
- Third-party review eligible
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| Record | Firm | Date | Builder |
|---|---|---|---|
| BRUSHRITE (K880442) | Pro Care Laboratories, Inc. | 1988-05-16 | + Add |
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Every clearance here is in the API, with alerts when new ones post.