The following data is part of a premarket notification filed by Hamilton Co. with the FDA for Microlab At.
| Device ID | K871945 |
| 510k Number | K871945 |
| Device Name: | MICROLAB AT |
| Classification | Device, Microtiter Diluting/dispensing |
| Applicant | HAMILTON CO. POST OFFICE BOX 10030 Reno, NV 89520 |
| Contact | Ken Lindner |
| Correspondent | Ken Lindner HAMILTON CO. POST OFFICE BOX 10030 Reno, NV 89520 |
| Product Code | JTC |
| CFR Regulation Number | 866.2500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-05-19 |
| Decision Date | 1987-05-29 |