K090209 is an FDA 510(k) clearance for the HEMOSIL LIQUID HEPARIN, HEPARIN CALIBRATORS AND LMW AND UF HEPARIN CONTROLS. This device is classified as a Assay, Heparin (Class II - Special Controls, product code KFF).
Submitted by Instrumentation Laboratory CO (Bedford, US). The FDA issued a Cleared decision on June 2, 2009, 125 days after receiving the submission on January 28, 2009.
This device falls under the Hematology FDA review panel. Regulated under 21 CFR 864.7525.
| 510(k) Number | K090209 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 28, 2009 |
| Decision Date | June 02, 2009 |
| Days to Decision | 125 days |
| Submission Type | Traditional |
| Review Panel | Hematology (HE) |
| Summary | Summary PDF |
| Product Code | KFF — Assay, Heparin |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 864.7525 |