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

Acid, Ferric Ion-Sulfuric, Cholesterol

21 CFR 862.1175 / Clinical Chemistry
FDA source (opens on fda.gov)

CHD is the FDA product code for Acid, Ferric Ion-Sulfuric, Cholesterol, a class I device type, regulated under 21 CFR 862.1175. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
CHD
Device name
Acid, Ferric Ion-Sulfuric, Cholesterol
Regulation
21 CFR 862.1175
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
3
Ingested recalls
0

Clearances, product code CHD

By decision year
3 clearances under product code CHD with a decision year between 1982 and 1984, 1982 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code CHD by decision year
YearClearances
19821
19831
19841

Applicants with the most clearances

Product code CHD
Applicants holding the most 510(k) clearances under product code CHD
ApplicantClearances
American Monitor Corp.1
Medical Specialties Inc.1
Omega Medical Electronics1

Companies listing this code with FDA

Companies whose registered establishments list this code