The following data is part of a premarket notification filed by Innovative Medical Systems, Inc. with the FDA for Mi Das 1000 Automatic Slide Stainer.
| Device ID | K821830 |
| 510k Number | K821830 |
| Device Name: | MI DAS 1000 AUTOMATIC SLIDE STAINER |
| Classification | Slide Stainer, Automated |
| Applicant | INNOVATIVE MEDICAL SYSTEMS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KPA |
| CFR Regulation Number | 864.3800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-06-22 |
| Decision Date | 1982-07-22 |