FLAME PHOTOMETER CALIBRATION STANDARDS— 510(k) K813505

Name: FDA 510(k) clearance K813505
Creator: U.S. Food and Drug Administration
Published: 1981-12-31

Substantially Equivalent

Fisher Scientific Co., LLC

FDA 510(k) clearance K813505 for FLAME PHOTOMETER CALIBRATION STANDARDS, Substantially Equivalent on 1981-12-31. Applicant: Fisher Scientific Co., LLC. Device class: 2.

Clearance details

Applicant: Fisher Scientific Co., LLC
Product code: Code JIS
Device class: Class 2
Regulation: 21 CFR 862.1150
Advisory panel: Clinical Chemistry
Date received: 1981-12-15
Decision date: 1981-12-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JIS

view all

K122126 — DIRECT LDL/HDL CHOLESTEROL CALIBRATOR2012-08-14
K061251 — DIMENSION VISTA TOTAL IRON BINDING CAPACITY CALIBRATOR2006-05-31
K060266 — DIMENSION IRON CALIBRATOR2006-03-09
K053104 — DIMENSION CARDIOPHASE HIGH SENSITIVITY C-REACTIVE PROTEIN CALIBRATOR2005-12-23
K032697 — DIMENSION TOTAL TRIIODOTHYRONINE CALIBRATOR (RC414)2003-11-07

More clearances from Fisher Scientific Co., LLC

view all

K930415 — MICROHEMATOCRIT ROTOR1993-03-23
K915825 — MARATHON 6K GENERAL-PURPOSE CENTRIFUGE1992-03-11
K915441 — MARATHON 13K/H MICROHEMATOCRIT CENTRIFUGE1992-01-08
K890534 — MODIFIED URIQUAL(TM) URINALYSIS CONTROL LEVEL 11989-03-08
K881275 — URIQUAL(TM) URINALYSIS CONTROLS (HUMAN) I & II1988-05-16

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