Submission Details
| 510(k) Number | K790709 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | April 12, 1979 |
| Decision Date | August 16, 1979 |
| Days to Decision | 126 days |
| Submission Type | Traditional |
| Review Panel | Immunology (IM) |
| Summary | — |
K790709 is an FDA 510(k) clearance for the ANTISERUM TO RABBIT IMMUNOGLOBULIN, a Igg (gamma Chain Specific), Antigen, Antiserum, Control (Class II — Special Controls, product code DFZ), submitted by Kent Laboratories, Inc. (Mchenry, US). The FDA issued a Cleared decision on August 16, 1979, 126 days after receiving the submission on April 12, 1979. This device falls under the Immunology review panel. Regulated under 21 CFR 866.5510.
| 510(k) Number | K790709 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | April 12, 1979 |
| Decision Date | August 16, 1979 |
| Days to Decision | 126 days |
| Submission Type | Traditional |
| Review Panel | Immunology (IM) |
| Summary | — |
| Product Code | DFZ — Igg (gamma Chain Specific), Antigen, Antiserum, Control |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 866.5510 |