Submission Details
| 510(k) Number | K843425 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | September 04, 1984 |
| Decision Date | October 02, 1984 |
| Days to Decision | 28 days |
| Submission Type | Traditional |
| Review Panel | Pathology (PA) |
| Summary | — |
K843425 is an FDA 510(k) clearance for the HARRIS HEMATOXYLIN, MERCURY FREE, ACID, a Hematoxylin Harris's (Class I — General Controls, product code HYK), submitted by Accra Laboratories, Inc. (Mchenry, US). The FDA issued a Cleared decision on October 2, 1984, 28 days after receiving the submission on September 4, 1984. This device falls under the Pathology review panel. Regulated under 21 CFR 864.1850.
| 510(k) Number | K843425 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | September 04, 1984 |
| Decision Date | October 02, 1984 |
| Days to Decision | 28 days |
| Submission Type | Traditional |
| Review Panel | Pathology (PA) |
| Summary | — |
| Product Code | HYK — Hematoxylin Harris's |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 864.1850 |