KLX
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Electroglottograph
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 874.1325
- Medical specialty
- Ear, Nose, Throat
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| Record | Firm | Date | Builder |
|---|---|---|---|
| ELECTROGLOTTOGRAPH (K990240) | Kay Elemetrics Corp. | 1999-03-11 | + Add |
| ELECTROGLOTTOGRAPH (K901609) | Glottal Ent., Inc. | 1990-06-28 | + Add |
| GLOTTAL FREQUENCY ANALYSER (K841832) | Teltec Electronic Equipment AB | 1984-07-18 | + Add |
| ELECTROGLOTTOGRAPH NAKED EGG BOXED EGG (K821079) | Ms. Kate Teaney | 1982-05-10 | + Add |
Track KLX automatically
Every clearance here is in the API, with alerts when new ones post.