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

Electrophoretic Method, Catecholamines

21 CFR 862.1165 / Clinical Chemistry
FDA source (opens on fda.gov)

CHT is the FDA product code for Electrophoretic Method, Catecholamines, a class I device type, regulated under 21 CFR 862.1165. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
CHT
Device name
Electrophoretic Method, Catecholamines
Regulation
21 CFR 862.1165
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
0

Clearances, product code CHT

By decision year
2 clearances under product code CHT with a decision year between 1976 and 1991, 1976 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code CHT by decision year
YearClearances
19761
19911

Applicants with the most clearances

Product code CHT
Applicants holding the most 510(k) clearances under product code CHT
ApplicantClearances
Eastman Kodak Company1
The Upjohn Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code