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

Conversion To Ferric Hydroxymates (Colorimetric), Fatty Acids

21 CFR 862.1290 / Clinical Chemistry
FDA source (opens on fda.gov)

JLG is the FDA product code for Conversion To Ferric Hydroxymates (Colorimetric), Fatty Acids, a class I device type, regulated under 21 CFR 862.1290. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
JLG
Device name
Conversion To Ferric Hydroxymates (Colorimetric), Fatty Acids
Regulation
21 CFR 862.1290
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
2
Ingested recalls
1

Clearances, product code JLG

By decision year
2 clearances under product code JLG with a decision year between 1976 and 1981, 1976 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JLG by decision year
YearClearances
19761
19811

Applicants with the most clearances

Product code JLG
Applicants holding the most 510(k) clearances under product code JLG
ApplicantClearances
Dennison Manufacturing Co.1
FUJIFILM Healthcare Americas Corporation1

Companies listing this code with FDA

Companies whose registered establishments list this code