AKERSCAN COLORIMETRIC ANALYZER— 510(k) K862908

Name: FDA 510(k) clearance K862908
Creator: U.S. Food and Drug Administration
Published: 1986-09-15

Substantially Equivalent

Akers Medical Technologies

FDA 510(k) clearance K862908 for AKERSCAN COLORIMETRIC ANALYZER, Substantially Equivalent on 1986-09-15. Applicant: Akers Medical Technologies. Device class: 1.

Clearance details

Applicant: Akers Medical Technologies
Product code: Code JJQ
Device class: Class 1
Regulation: 21 CFR 862.2300
Advisory panel: Clinical Chemistry
Date received: 1986-07-31
Decision date: 1986-09-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cherry Hill, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JJQ

view all

K013371 — UBIT-IR300 INFRARED SPECTROMETRY SYSTEM2001-12-21
K980120 — DIGENE DML 2000 MICROPLATE LUMINOMETER1998-02-06
K973938 — ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READER1998-02-04
K974762 — STAT TRACKS1998-01-28
K962113 — ANTHOS PHACTS VERSION MICROPLATE READER1996-11-05

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