Tissue Culture/Bacteriological Petri Dishes
FDA 510(k) K871483 · Isratech Marketing Corp.
510(k) numberK871483
Submission
- Device name
- Tissue Culture/Bacteriological Petri Dishes
- Applicant
- Isratech Marketing Corp.
New York, NY, US - Received
- April 15, 1987
- Decision date
- April 29, 1987
- 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 |
| 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 |
| K790958 | 120 Well Histo-PlateKIZ · Traditional | Dynatech Laboratories, Inc. | 06/28/1979SE |
| K781792 | Pressurizer, Exeter CementKIZ · Traditional | Howmedica Corp. | 02/08/1979SE |
More from Howmedica Corp.
| 510(k) | Device | Decision |
|---|---|---|
| K896165 | Sterile Hypoallergenic Surgeons' GlovesKGO · Traditional | 11/22/1989SE |
Questions and answers
When was Tissue Culture/Bacteriological Petri Dishes cleared by the FDA?
Tissue Culture/Bacteriological Petri Dishes (K871483) received a 510(k) decision of Substantially Equivalent on April 29, 1987, 14 days after the submission was received.
What is the product code of K871483?
The FDA product code is KIZ – Dish, Tissue Culture, a Class I (low risk) device regulated under 21 CFR 864.2240.