Submission Details
| 510(k) Number | K892369 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | April 06, 1989 |
| Decision Date | June 02, 1989 |
| Days to Decision | 57 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | — |
K892369 is an FDA 510(k) clearance for the MULTI-PROBE HEAD PLUS, a Device, Microtiter Diluting/dispensing (Class I — General Controls, product code JTC), submitted by Hamilton Co. (Reno, US). The FDA issued a Cleared decision on June 2, 1989, 57 days after receiving the submission on April 6, 1989. This device falls under the Microbiology review panel. Regulated under 21 CFR 866.2500.
| 510(k) Number | K892369 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | April 06, 1989 |
| Decision Date | June 02, 1989 |
| Days to Decision | 57 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 |