Product code CFM— Clinical Chemistry
ABBOTT A-GENT IRON REAGENT KIT
- Classification name
- Bathophenanthroline, Colorimetry, Iron (Non-Heme)
- Device class
- Class 1
- Regulation
- 21 CFR 862.1410
- Advisory panel
- Clinical Chemistry
- Total cleared
- 21
- First cleared
- Most recent
Market context for product code CFM
FDA has cleared devices under product code CFM between 1979 and 1999, filed by 15 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1999
- 1998
- 1993
- 1991
- 1990
- 1989
- 1987
- 1986
- 1985
- 1984
- 1983
- 1982
- 1981
- 1979
Top applicants under product code CFM
Recent clearances under product code CFM
- K984119 — WAKO L-TYPE FE, WAKO L-TYPE CALIBRATOR
- K981581 — IRON
- K932871 — UIBC FOR DISCREET RANDOM ACCESS ANALYZER
- K913705 — ABBOTT QLUICKSTART IRON TEST, ITEM #5A29
- K912912 — SYNERMED SERUM IRON-600 REAGENT KIT
- K902918 — SYNERMED SERUM IRON REAGENT KIT
- K895047 — CLINISTAT POTASSIUM REAGENT TEST
- K891155 — IRON REAGENT
- K873120 — ABBOTT A-GENT IRON REAGENT KIT
- K861602 — TOTAL IRON BINDING CAPACITY PROCEDURE
- K854305 — DART IRON & IRON BINDING CAPACITY REAGENT
- K852583 — DATA CHEM IRON PROCEDURE
- K842155 — SERUM IRON & SERUM IRON BINDING CAPACI
- K842156 — SERUM IRON & SERUM IRON BINDING CAPACITY
- K842505 — TDX REA IRON DIAGNOSTIC KIT
- K840485 — TOTAL IRON UIBC/TIBC ASSAY
- K834396 — DIRECT IRON REAGENT SET
- K830564 — FEB TEST
- K820629 — CORNING 902 SODIUM POTASSIUM ANALYZER
- K810085 — IRON KIT
- K792406 — ELVI SERUM IRON
Data sourced from openFDA. This site is unofficial and independent of the FDA.