THE CEN-SLIDE(TM) CENTRIFUGE TUBE— 510(k) K891604

Name: FDA 510(k) clearance K891604
Creator: U.S. Food and Drug Administration
Published: 1989-06-16

Substantially Equivalent

Davstar California, Inc.

FDA 510(k) clearance K891604 for THE CEN-SLIDE(TM) CENTRIFUGE TUBE, Substantially Equivalent on 1989-06-16. Applicant: Davstar California, Inc.. Device class: 1.

Clearance details

Applicant: Davstar California, Inc.
Product code: Code KEW
Device class: Class 1
Regulation: 21 CFR 864.3010
Advisory panel: Pathology
Date received: 1989-03-20
Decision date: 1989-06-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lawndale, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KEW

view all

K890042 — MICROSCOPE SLIDES PRECOATED1989-01-13
K882357 — MICROSCOPE SLIDES PRECOATED W/HISTOGRIP & POLY-LY1988-06-16
K831065 — SECTIONING AID KIT1983-06-08
K820100 — FROSTED GLASS SLIDES1982-03-04
K813242 — QUANTIMETRIC 2 TEST KIT1981-12-02

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