510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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CFMClass I

Bathophenanthroline, Colorimetry, Iron (Non-Heme)

21 CFR 862.1410 / Clinical Chemistry
FDA source (opens on fda.gov)

CFM is the FDA product code for Bathophenanthroline, Colorimetry, Iron (Non-Heme), a class I device type, regulated under 21 CFR 862.1410. As of , FDA records hold 21 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
CFM
Device name
Bathophenanthroline, Colorimetry, Iron (Non-Heme)
Regulation
21 CFR 862.1410
Device class
Class I
Review panel
Clinical Chemistry
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
21
Ingested recalls
0

Clearances, product code CFM

By decision year
21 clearances under product code CFM with a decision year between 1979 and 1999, 1984 the highest year at 5.
Show the numbers
510(k) clearances under FDA product code CFM by decision year
YearClearances
19791
19811
19821
19831
19845
19852
19861
19871
19892
19901
19912
19931
19981
19991

Applicants with the most clearances

Product code CFM
Applicants holding the most 510(k) clearances under product code CFM
ApplicantClearances
Abbott Medical3
Data Medical Associates, Inc.2
Diagnostic Chemicals, Ltd. (USA)2
Synermed, Inc.2
FUJIFILM Healthcare Americas Corporation2
Bio-Analytics Laboratories, Inc.1
Catachem, Inc.1
Corning Medical & Scientific1
Coulter Electronics, Inc.1
Em Diagnostic Systems, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code