The following data is part of a premarket notification filed by Gelco Diagnostics, Inc. with the FDA for Rabbit Anti-human Antithrombin Iii.
| Device ID | K832268 |
| 510k Number | K832268 |
| Device Name: | RABBIT ANTI-HUMAN ANTITHROMBIN III |
| Classification | Antithrombin Iii Quantitation |
| Applicant | GELCO DIAGNOSTICS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JBQ |
| CFR Regulation Number | 864.7060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-06-30 |
| Decision Date | 1983-08-12 |