120 Well Histo-Plate

FDA 510(k) K790958 · Dynatech Laboratories, Inc.

Substantially Equivalent

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)

Official FDA 510(k) record

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)DeviceApplicantDecision
K890542Multiwell Culture Plate InsertsKIZ · Traditional Bd Becton Dickinson Vacutainer Systems Preanalytic02/14/1989SE
K873891Tissue Culture DishesKIZ · Traditional Nunc, Inc.11/25/1987SE
K871483Tissue Culture/Bacteriological Petri DishesKIZ · Traditional Isratech Marketing Corp.04/29/1987SE
K854724Cekk-Adhesive Matrix-Multiple Well Plate Cam-PlateKIZ · Traditional Lifetrac, Inc.12/13/1985SE
K853634Corning Cell Wells-Multiple Well PlatesKIZ · Traditional Corning Medical & Scientific09/16/1985SE
K821687Removawell Tissue Culture Plate W/LidKIZ · Traditional Dynatech Corp.06/24/1982SE
K781792Pressurizer, Exeter CementKIZ · Traditional Howmedica Corp.02/08/1979SE

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K923456Microlite Microtiter Plate Luminometer ML3000JJQ · Traditional 10/13/1992SE
K915896Microlite Microtiter Plate Luminometer ML2250/MODIJJQ · Traditional 05/04/1992SE
K920888Microlite Microtiter Plate Luminometer ML2200KHO · Traditional 03/19/1992SE
K913590Microlite ML 1000 Microtiter Plate LuminometerJJQ · Traditional 10/25/1991SE
K895313Microlite ML 1000 (Model 3) Microplate LuminometerJJQ · Traditional 10/17/1989SE
K894645Immulon 1,2,3,AND 4 Dividastrips TMJTC · Traditional 10/17/1989SE
K894687Dynatech 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.