The following data is part of a premarket notification filed by Lee Pharmaceuticals with the FDA for Mercury Disp. Capsule.
| Device ID | K781243 |
| 510k Number | K781243 |
| Device Name: | MERCURY DISP. CAPSULE |
| Classification | Capsule, Dental, Amalgam |
| Applicant | LEE PHARMACEUTICALS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DZS |
| CFR Regulation Number | 872.3110 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-06-12 |
| Decision Date | 1978-09-20 |