IYW
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Scanner, Rectilinear, Nuclear
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 892.1300
- Medical specialty
- Radiology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| POLYSCAN DIGITAL SCANNER (K944684) | Mse Medizintechnik GmbH & Co. KG | 1995-05-15 |
| RECTILINEAR SCANNER MODEL #187-270 (K895799) | Atomic Products Corp. | 1990-02-01 |
| POLYSCAN DIGITAL SCANNER (K882453) | Medical and Scientific Enterprises, Inc. | 1988-11-23 |
| IMAGER, BODY SECTION, RADIONUCLIDE (K780395) | Union Carbide Corp. | 1978-03-31 |
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Every clearance here is in the API, with alerts when new ones post.