Submission Details
| 510(k) Number | K895826 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | October 02, 1989 |
| Decision Date | October 30, 1989 |
| Days to Decision | 28 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | — |
K895826 is an FDA 510(k) clearance for the INNOFLUOR DIGOXIN CALIBRATOR SET, a Calibrators, Drug Specific (Class II — Special Controls, product code DLJ), submitted by Innotron of Oregon, Inc. (Portland, US). The FDA issued a Cleared decision on October 30, 1989, 28 days after receiving the submission on October 2, 1989. This device falls under the Toxicology review panel. Regulated under 21 CFR 862.3200.
| 510(k) Number | K895826 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | October 02, 1989 |
| Decision Date | October 30, 1989 |
| Days to Decision | 28 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 |