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 |