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

Electrode, Electrocardiograph, Multi-Function

21 CFR 870.2360 / Cardiovascular
FDA source (opens on fda.gov)

MLN is the FDA product code for Electrode, Electrocardiograph, Multi-Function, a class II device type, regulated under 21 CFR 870.2360. As of , FDA records hold no 510(k) clearances under this code and 9 recalls.

Classification record

Product code
MLN
Device name
Electrode, Electrocardiograph, Multi-Function
Regulation
21 CFR 870.2360
Device class
Class II
Review panel
Cardiovascular
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
9

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 19 companies shown, in name order