The following data is part of a premarket notification filed by Kent Laboratories, Inc. with the FDA for Determ. Size 72 Radial-human Igd.
| Device ID | K831956 |
| 510k Number | K831956 |
| Device Name: | DETERM. SIZE 72 RADIAL-HUMAN IGD |
| Classification | Igd, Antigen, Antiserum, Control |
| Applicant | KENT LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CZJ |
| CFR Regulation Number | 866.5510 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-06-17 |
| Decision Date | 1983-07-18 |