Submission Details
| 510(k) Number | K810039 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | January 09, 1981 |
| Decision Date | January 28, 1981 |
| Days to Decision | 19 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | — |
K810039 is an FDA 510(k) clearance for the MIC-2000 INOCULUM TRAY LID, a Device, Microtiter Diluting/dispensing (Class I — General Controls, product code JTC), submitted by Dynatech Corp. (Mchenry, US). The FDA issued a Cleared decision on January 28, 1981, 19 days after receiving the submission on January 9, 1981. This device falls under the Microbiology review panel. Regulated under 21 CFR 866.2500.
| 510(k) Number | K810039 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | January 09, 1981 |
| Decision Date | January 28, 1981 |
| Days to Decision | 19 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | — |
| Product Code | JTC — Device, Microtiter Diluting/dispensing |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 866.2500 |