Cekk-Adhesive Matrix-Multiple Well Plate Cam-Plate
FDA 510(k) K854724 · Lifetrac, Inc.
510(k) numberK854724
Submission
- Device name
- Cekk-Adhesive Matrix-Multiple Well Plate Cam-Plate
- Applicant
- Lifetrac, Inc.
Washington, DC, US - Received
- November 22, 1985
- Decision date
- December 13, 1985
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- KIZ – Dish, Tissue Culture
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 864.2240
- Specialty
- Hematology
Other 510(k)s with product code KIZ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K890542 | Multiwell Culture Plate InsertsKIZ · Traditional | Bd Becton Dickinson Vacutainer Systems Preanalytic | 02/14/1989SE |
| K873891 | Tissue Culture DishesKIZ · Traditional | Nunc, Inc. | 11/25/1987SE |
| K871483 | Tissue Culture/Bacteriological Petri DishesKIZ · Traditional | Isratech Marketing Corp. | 04/29/1987SE |
| K853634 | Corning Cell Wells-Multiple Well PlatesKIZ · Traditional | Corning Medical & Scientific | 09/16/1985SE |
| K821687 | Removawell Tissue Culture Plate W/LidKIZ · Traditional | Dynatech Corp. | 06/24/1982SE |
| K790958 | 120 Well Histo-PlateKIZ · Traditional | Dynatech Laboratories, Inc. | 06/28/1979SE |
| K781792 | Pressurizer, Exeter CementKIZ · Traditional | Howmedica Corp. | 02/08/1979SE |
Questions and answers
When was Cekk-Adhesive Matrix-Multiple Well Plate Cam-Plate cleared by the FDA?
Cekk-Adhesive Matrix-Multiple Well Plate Cam-Plate (K854724) received a 510(k) decision of Substantially Equivalent on December 13, 1985, 21 days after the submission was received.
What is the product code of K854724?
The FDA product code is KIZ – Dish, Tissue Culture, a Class I (low risk) device regulated under 21 CFR 864.2240.