Brillette Model
FDA 510(k) K842835 · Cillus Company, Inc.
510(k) numberK842835
Submission
- Device name
- Brillette Model
- Applicant
- Cillus Company, Inc.
Novato, CA, US - Received
- July 20, 1984
- Decision date
- November 21, 1984
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- HOI – Spectacle, Magnifying
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 886.5840
- Specialty
- Ophthalmic
Other 510(k)s with product code HOI
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K943613 | NilHOI · Traditional | Sing Wah International Enterprises , Ltd. | 09/21/1994SE |
| K930435 | Spectacle FramesHOI · Traditional | Venis DI A. Vendrame | 09/20/1993SE |
| K931328 | Pyramid Sunglasses/Pyramid Reading GlassesHOI · Traditional | Pyramid | 08/10/1993SE |
| K910329 | SunglassesHOI · Traditional | Cutler & Gross Sloan Optical , Ltd. | 03/12/1991SE |
| K854854 | Systems of Sight Low Vision EyewareHOI · Traditional | Int'L Eye Care, Inc. | 02/04/1986SE |
| K844716 | Magnifying Spectacles W/Plastic LensesHOI · Traditional | Gazelle Corp. | 01/03/1985SE |
| K844038 | Visitec Magnifying SpectaclesHOI · Traditional | Visitec Co. | 11/29/1984SE |
| K820732 | La Vel Lateral View Extension LensHOI · Traditional | Peter M. Tolliver | 05/03/1982SE |
| K813548 | Uvex Mini-SpecsHOI · Traditional | Bacou USA, Inc. and Uvex Safety, Inc. | 03/02/1982SE |
| K801733 | Fenzl ReticleHOI · Traditional | Robert E. Fenzl, M.D. | 09/16/1980SE |
Questions and answers
When was Brillette Model cleared by the FDA?
Brillette Model (K842835) received a 510(k) decision of Substantially Equivalent on November 21, 1984, 124 days after the submission was received.
What is the product code of K842835?
The FDA product code is HOI – Spectacle, Magnifying, a Class I (low risk) device regulated under 21 CFR 886.5840.