K900506 is an FDA 510(k) clearance for the MODIFIED COATRON II AND COATRON JR.. This device is classified as a System, Multipurpose For In Vitro Coagulation Studies (Class II - Special Controls, product code JPA).
Submitted by Astral Medical Systems (Indianapolis, US). The FDA issued a Cleared decision on March 12, 1990, 38 days after receiving the submission on February 2, 1990.
This device falls under the Hematology FDA review panel. Regulated under 21 CFR 864.5425.
| 510(k) Number | K900506 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 02, 1990 |
| Decision Date | March 12, 1990 |
| Days to Decision | 38 days |
| Submission Type | Traditional |
| Review Panel | Hematology (HE) |
| Summary | — |
| Product Code | JPA — System, Multipurpose For In Vitro Coagulation Studies |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 864.5425 |