The following data is part of a premarket notification filed by Litton Bionetics with the FDA for Toxo Bio-bead Titration Kit.
| Device ID | K801720 |
| 510k Number | K801720 |
| Device Name: | TOXO BIO-BEAD TITRATION KIT |
| Classification | Antigens, If, Toxoplasma Gondii |
| Applicant | LITTON BIONETICS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GLZ |
| CFR Regulation Number | 866.3780 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-07-23 |
| Decision Date | 1980-09-16 |