K021023 is an FDA 510(k) clearance for the HEMOSIL NORMAL CONTROL (ASSAYED). This device is classified as a Plasma, Coagulation Control (Class II - Special Controls, product code GGN).
Submitted by Instrumentation Laboratory CO (Bedford, US). The FDA issued a Cleared decision on May 14, 2002, 46 days after receiving the submission on March 29, 2002.
This device falls under the Hematology FDA review panel. Regulated under 21 CFR 864.5425.
| 510(k) Number | K021023 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 29, 2002 |
| Decision Date | May 14, 2002 |
| Days to Decision | 46 days |
| Submission Type | Traditional |
| Review Panel | Hematology (HE) |
| Summary | Summary PDF |
| Product Code | GGN — Plasma, Coagulation Control |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 864.5425 |