The following data is part of a premarket notification filed by Preventive Diagnostics Corp. with the FDA for Preserv Mf Fixative 15ml.
| Device ID | K840086 |
| 510k Number | K840086 |
| Device Name: | PRESERV MF FIXATIVE 15ML |
| Classification | Device, Specimen Collection |
| Applicant | PREVENTIVE DIAGNOSTICS CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LIO |
| CFR Regulation Number | 866.2900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-01-10 |
| Decision Date | 1984-01-30 |