The following data is part of a premarket notification filed by Dynatech Cryomedical Co. with the FDA for Automated Slide Spinner.
| Device ID | K771898 |
| 510k Number | K771898 |
| Device Name: | AUTOMATED SLIDE SPINNER |
| Classification | Spinner, Slide, Automated |
| Applicant | DYNATECH CRYOMEDICAL CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GKJ |
| CFR Regulation Number | 864.5850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-10-06 |
| Decision Date | 1977-10-18 |