The following data is part of a premarket notification filed by Dutchland Laboratories, Inc. with the FDA for Rabbit Complement.
| Device ID | K812522 |
| 510k Number | K812522 |
| Device Name: | RABBIT COMPLEMENT |
| Classification | Reagent, Complement |
| Applicant | DUTCHLAND LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KTQ |
| CFR Regulation Number | 866.4100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-09-02 |
| Decision Date | 1981-09-23 |