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

Chromatographic/Fluorometric Method, Catecholamines

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

CHQ is the FDA product code for Chromatographic/Fluorometric Method, Catecholamines, a class I device type, regulated under 21 CFR 862.1165. As of , FDA records hold 10 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
CHQ
Device name
Chromatographic/Fluorometric 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
10
Ingested recalls
0

Clearances, product code CHQ

By decision year
10 clearances under product code CHQ with a decision year between 1986 and 2005, 1986 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code CHQ by decision year
YearClearances
19861
19881
19891
19931
19941
19951
19961
19971
20041
20051

Applicants with the most clearances

Product code CHQ
Applicants holding the most 510(k) clearances under product code CHQ
ApplicantClearances
Bioanalytical Systems, Inc.3
Bio-Rad2
Esa, Inc.2
Esa, Inc.1
Ibl GmbH1
Whale Scientific, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code