K870390 is an FDA 510(k) clearance for the PHENOBARBITAL (FPIA) CALIBRATOR KIT. This device is classified as a Calibrators, Drug Specific (Class II - Special Controls, product code DLJ).
Submitted by Windsor Laboratories, Inc. (Garland, US). The FDA issued a Cleared decision on April 1, 1987, 61 days after receiving the submission on January 30, 1987.
This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3200.
| 510(k) Number | K870390 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 30, 1987 |
| Decision Date | April 01, 1987 |
| Days to Decision | 61 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | — |
| Product Code | DLJ — Calibrators, Drug Specific |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.3200 |