The following data is part of a premarket notification filed by Connecticut Diagnostics, Ltd. with the FDA for Cdl Isotonic Diluent.
| Device ID | K822501 |
| 510k Number | K822501 |
| Device Name: | CDL ISOTONIC DILUENT |
| Classification | Diluent, Blood Cell |
| Applicant | CONNECTICUT DIAGNOSTICS, LTD. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GIF |
| CFR Regulation Number | 864.8200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-08-18 |
| Decision Date | 1982-09-17 |