CEKK-ADHESIVE MATRIX-MULTIPLE WELL PLATE CAM-PLATE— 510(k) K854724

Name: FDA 510(k) clearance K854724
Creator: U.S. Food and Drug Administration
Published: 1985-12-13

Substantially Equivalent

Lifetrac, Inc.

FDA 510(k) clearance K854724 for CEKK-ADHESIVE MATRIX-MULTIPLE WELL PLATE CAM-PLATE, Substantially Equivalent on 1985-12-13. Applicant: Lifetrac, Inc.. Device class: 1.

Clearance details

Applicant: Lifetrac, Inc.
Product code: Code KIZ
Device class: Class 1
Regulation: 21 CFR 864.2240
Advisory panel: Hematology
Date received: 1985-11-22
Decision date: 1985-12-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KIZ

view all

K890542 — MULTIWELL CULTURE PLATE INSERTS1989-02-14
K873891 — TISSUE CULTURE DISHES1987-11-25
K871483 — TISSUE CULTURE/BACTERIOLOGICAL PETRI DISHES1987-04-29
K853634 — CORNING CELL WELLS-MULTIPLE WELL PLATES1985-09-16
K821687 — REMOVAWELL TISSUE CULTURE PLATE W/LID1982-06-24

Data sourced from openFDA. This site is unofficial and independent of the FDA.