The following data is part of a premarket notification filed by Hamilton Co. with the FDA for Multi-probe Head Plus.
| Device ID | K892369 |
| 510k Number | K892369 |
| Device Name: | MULTI-PROBE HEAD PLUS |
| Classification | Device, Microtiter Diluting/dispensing |
| Applicant | HAMILTON CO. 4960 ENERGY WAY Reno, NV 89502 -0012 |
| Contact | Ken Lindner |
| Correspondent | Ken Lindner HAMILTON CO. 4960 ENERGY WAY Reno, NV 89502 -0012 |
| Product Code | JTC |
| CFR Regulation Number | 866.2500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-04-06 |
| Decision Date | 1989-06-02 |