The following data is part of a premarket notification filed by Surgipath with the FDA for Acrytol, Mounting Medium.
| Device ID | K810323 |
| 510k Number | K810323 |
| Device Name: | ACRYTOL, MOUNTING MEDIUM |
| Classification | Media, Mounting, Oil Soluble |
| Applicant | SURGIPATH 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KEP |
| CFR Regulation Number | 864.4010 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-02-06 |
| Decision Date | 1981-03-06 |