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

Colorimetric, Xylose

21 CFR 862.1820 / Clinical Chemistry
FDA source (opens on fda.gov)

JOC is the FDA product code for Colorimetric, Xylose, a class I device type, regulated under 21 CFR 862.1820. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
JOC
Device name
Colorimetric, Xylose
Regulation
21 CFR 862.1820
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
1
Ingested recalls
0

Clearances, product code JOC

By decision year
1 clearance under product code JOC with a decision year between 1999 and 1999, 1999 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JOC by decision year
YearClearances
19991

Applicants with the most clearances

Product code JOC
Applicants holding the most 510(k) clearances under product code JOC
ApplicantClearances
Great Smokies Diagnostic Laboratory1

Companies listing this code with FDA

Companies whose registered establishments list this code