120 Well Histo-Plate
FDA 510(k) K790958 · Dynatech Laboratories, Inc.
510(k) numberK790958
Submission
- Device name
- 120 Well Histo-Plate
- Applicant
- Dynatech Laboratories, Inc.
Mchenry, IL, US - Received
- May 22, 1979
- Decision date
- June 28, 1979
- 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 |
| K854724 | Cekk-Adhesive Matrix-Multiple Well Plate Cam-PlateKIZ · Traditional | Lifetrac, Inc. | 12/13/1985SE |
| 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 |
| K781792 | Pressurizer, Exeter CementKIZ · Traditional | Howmedica Corp. | 02/08/1979SE |
More from Howmedica Corp.
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| K962265 | MLX Microtiter Plate LuminometerJSE · Traditional | 07/25/1996SE |
| K934111 | MR7000 with Time Manager Software (TMS)JQP · Traditional | 11/02/1994SE |
| K943701 | MRX Microplate ReaderJJQ · Traditional | 10/20/1994SE |
| K923456 | Microlite Microtiter Plate Luminometer ML3000JJQ · Traditional | 10/13/1992SE |
| K915896 | Microlite Microtiter Plate Luminometer ML2250/MODIJJQ · Traditional | 05/04/1992SE |
| K920888 | Microlite Microtiter Plate Luminometer ML2200KHO · Traditional | 03/19/1992SE |
| K913590 | Microlite ML 1000 Microtiter Plate LuminometerJJQ · Traditional | 10/25/1991SE |
| K895313 | Microlite ML 1000 (Model 3) Microplate LuminometerJJQ · Traditional | 10/17/1989SE |
| K894645 | Immulon 1,2,3,AND 4 Dividastrips TMJTC · Traditional | 10/17/1989SE |
| K894687 | Dynatech MR 5000, Catalog #011-976-0600JJQ · Traditional | 08/31/1989SE |
Questions and answers
When was 120 Well Histo-Plate cleared by the FDA?
120 Well Histo-Plate (K790958) received a 510(k) decision of Substantially Equivalent on June 28, 1979, 37 days after the submission was received.
What is the product code of K790958?
The FDA product code is KIZ – Dish, Tissue Culture, a Class I (low risk) device regulated under 21 CFR 864.2240.