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

Electrode, Ion Specific, Magnesium

21 CFR 862.1495 / Clinical Chemistry
FDA source (opens on fda.gov)

CFA is the FDA product code for Electrode, Ion Specific, Magnesium, a class I device type, regulated under 21 CFR 862.1495. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
CFA
Device name
Electrode, Ion Specific, Magnesium
Regulation
21 CFR 862.1495
Device class
Class I
Review panel
Clinical Chemistry
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
2
Ingested recalls
0

Clearances, product code CFA

By decision year
2 clearances under product code CFA with a decision year between 1985 and 1986, 1985 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code CFA by decision year
YearClearances
19851
19861

Applicants with the most clearances

Product code CFA
Applicants holding the most 510(k) clearances under product code CFA
ApplicantClearances
Bio-Analytics Laboratories, Inc.1
Data Medical Associates, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code