The following data is part of a premarket notification filed by Analytical Products, Inc. with the FDA for Dynex Blood Gas Quality Control Sys..
| Device ID | K780144 |
| 510k Number | K780144 |
| Device Name: | DYNEX BLOOD GAS QUALITY CONTROL SYS. |
| Classification | Controls For Blood-gases, (assayed And Unassayed) |
| Applicant | ANALYTICAL PRODUCTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JJS |
| CFR Regulation Number | 862.1660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-01-24 |
| Decision Date | 1978-05-26 |