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

Gas Chromatograph, Carbon-Monoxide

21 CFR 862.3220 / Clinical Toxicology
FDA source (opens on fda.gov)

JKT is the FDA product code for Gas Chromatograph, Carbon-Monoxide, a class I device type, regulated under 21 CFR 862.3220. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JKT
Device name
Gas Chromatograph, Carbon-Monoxide
Regulation
21 CFR 862.3220
Device class
Class I
Review panel
Clinical Toxicology
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 JKT

By decision year
2 clearances under product code JKT with a decision year between 1983 and 1983, 1983 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code JKT by decision year
YearClearances
19832

Applicants with the most clearances

Product code JKT
Applicants holding the most 510(k) clearances under product code JKT
ApplicantClearances
Rna Medical Corp.1
Shaban Mfg. Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code