Submission Details
| 510(k) Number | K800325 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | February 12, 1980 |
| Decision Date | February 26, 1980 |
| Days to Decision | 14 days |
| Submission Type | Traditional |
| Review Panel | Pathology (PA) |
| Summary | — |
K800325 is an FDA 510(k) clearance for the VOLU-SOL HISTO./CYTO. STAIN MOD. #EA65, a Stain, Papanicolau (Class I — General Controls, product code HZJ), submitted by Volu Sol Medical Industries (Mchenry, US). The FDA issued a Cleared decision on February 26, 1980, 14 days after receiving the submission on February 12, 1980. This device falls under the Pathology review panel. Regulated under 21 CFR 864.1850.
| 510(k) Number | K800325 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | February 12, 1980 |
| Decision Date | February 26, 1980 |
| Days to Decision | 14 days |
| Submission Type | Traditional |
| Review Panel | Pathology (PA) |
| Summary | — |
| Product Code | HZJ — Stain, Papanicolau |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 864.1850 |