The following data is part of a premarket notification filed by Kingswood Laboratories, Inc. with the FDA for Throat Moi-stir.
| Device ID | K840807 |
| 510k Number | K840807 |
| Device Name: | THROAT MOI-STIR |
| Classification | Saliva, Artificial |
| Applicant | KINGSWOOD LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LFD |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-02-24 |
| Decision Date | 1984-05-25 |