Tissue Culture Dishes

FDA 510(k) K873891 · Nunc, Inc.

Substantially Equivalent

510(k) numberK873891

Submission

Device name
Tissue Culture Dishes
Applicant
Nunc, Inc.
Riverside, CA, US
Received
September 23, 1987
Decision date
November 25, 1987
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
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
K790958120 Well Histo-PlateKIZ · Traditional Dynatech Laboratories, Inc.06/28/1979SE
K781792Pressurizer, Exeter CementKIZ · Traditional Howmedica Corp.02/08/1979SE

More from Howmedica Corp.

510(k)DeviceDecision
K873890Tissue Culture FlasksKJA · Traditional 11/25/1987SE
K873889Tissue Culture TubesKJA · Traditional 11/25/1987SE

Questions and answers

When was Tissue Culture Dishes cleared by the FDA?

Tissue Culture Dishes (K873891) received a 510(k) decision of Substantially Equivalent on November 25, 1987, 63 days after the submission was received.

What is the product code of K873891?

The FDA product code is KIZ – Dish, Tissue Culture, a Class I (low risk) device regulated under 21 CFR 864.2240.