The following data is part of a premarket notification filed by Gelco Diagnostics, Inc. with the FDA for Goat Anti-human Lamba.
| Device ID | K832270 |
| 510k Number | K832270 |
| Device Name: | GOAT ANTI-HUMAN LAMBA |
| Classification | Lambda, Antigen, Antiserum, Control |
| Applicant | GELCO DIAGNOSTICS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DEH |
| CFR Regulation Number | 866.5550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-06-30 |
| Decision Date | 1983-10-31 |