IYH
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Generator, Dermatological (Grenz Ray), Therapeutic X-Ray
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 892.5900
- Medical specialty
- Radiology
- Flags
- Third-party review eligible
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| Record | Firm | Date | Builder |
|---|---|---|---|
| X-CEL X-RAY MODELS ORT90W, ORT90M AND ORT90R (K871116) | X-Cel X-Ray Corp. | 1987-05-14 | + Add |
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Every clearance here is in the API, with alerts when new ones post.