Anterior/Posterior Restorative Liquid
FDA 510(k) K790822 · Scientific Pharmaceuticals, Inc.
510(k) numberK790822
Submission
- Device name
- Anterior/Posterior Restorative Liquid
- Applicant
- Scientific Pharmaceuticals, Inc.
Mchenry, IL, US - Received
- May 1, 1979
- Decision date
- July 6, 1979
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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| K261357 | Grandio disc multicolorEBF · Traditional | Voco GmbH | 04/27/2026SE |
| K261356 | Dura-CrownEBF · Special | Hangzhou SHINING3D Dental Technology Co., Ltd. | 04/27/2026SE |
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Questions and answers
When was Anterior/Posterior Restorative Liquid cleared by the FDA?
Anterior/Posterior Restorative Liquid (K790822) received a 510(k) decision of Substantially Equivalent on July 6, 1979, 66 days after the submission was received.
What is the product code of K790822?
The FDA product code is EBF – Material, Tooth Shade, Resin, a Class II (moderate risk) device regulated under 21 CFR 872.3690.