K193204 is an FDA 510(k) clearance for the Cryocheck Chromogenic Factor VIII. This device is classified as a Test, Qualitative And Quantitative Factor Deficiency (Class II - Special Controls, product code GGP).
Submitted by Precision Biologic (Darmouth, CA). The FDA issued a Cleared decision on July 17, 2020, 240 days after receiving the submission on November 20, 2019.
This device falls under the Hematology FDA review panel. Regulated under 21 CFR 864.7290.
| 510(k) Number | K193204 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 20, 2019 |
| Decision Date | July 17, 2020 |
| Days to Decision | 240 days |
| Submission Type | Traditional |
| Review Panel | Hematology (HE) |
| Summary | Summary PDF |
| Product Code | GGP - Test, Qualitative And Quantitative Factor Deficiency |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 864.7290 |