GLG
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Platelet Counting, Manual
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 864.6160
- Medical specialty
- Hematology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| REES & ECKER DILUTION FLUID (K842921) | E K Ind., Inc. | 1984-09-07 |
| LABTRONIX PLATELET COUNTER(L/O/C.) (K811084) | Labtronix Corp. | 1981-07-23 |
| PLATELET KIT (K772105) | Streck Laboratories, Inc. | 1977-11-30 |
Track GLG automatically
Every clearance here is in the API, with alerts when new ones post.