Submission Details
| 510(k) Number | K811794 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 24, 1981 |
| Decision Date | July 28, 1981 |
| Days to Decision | 34 days |
| Submission Type | Traditional |
| Review Panel | Hematology (HE) |
| Summary | — |
K811794 is an FDA 510(k) clearance for the 37% FORMALDEHYDE, a Formaldehyde (formalin, Formol) (Class I — General Controls, product code IGG), submitted by Richard-Allan Medical Ind., Inc. (Mchenry, US). The FDA issued a Cleared decision on July 28, 1981, 34 days after receiving the submission on June 24, 1981. This device falls under the Hematology review panel. Regulated under 21 CFR 864.4010.
| 510(k) Number | K811794 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 24, 1981 |
| Decision Date | July 28, 1981 |
| Days to Decision | 34 days |
| Submission Type | Traditional |
| Review Panel | Hematology (HE) |
| Summary | — |
| Product Code | IGG — Formaldehyde (formalin, Formol) |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 864.4010 |