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

Method, Metallic Reduction, Glucose (Urinary, Non-Quantitative)

21 CFR 862.1340 / Clinical Chemistry
FDA source (opens on fda.gov)

JIM is the FDA product code for Method, Metallic Reduction, Glucose (Urinary, Non-Quantitative), a class II device type, regulated under 21 CFR 862.1340. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JIM
Device name
Method, Metallic Reduction, Glucose (Urinary, Non-Quantitative)
Regulation
21 CFR 862.1340
Device class
Class II
Review panel
Clinical Chemistry
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
2
Ingested recalls
0

Clearances, product code JIM

By decision year
2 clearances under product code JIM with a decision year between 1979 and 1990, 1979 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JIM by decision year
YearClearances
19791
19901

Applicants with the most clearances

Product code JIM
Applicants holding the most 510(k) clearances under product code JIM
ApplicantClearances
Boehringer Mannheim Corp.1
Hichem Diagnostics1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code JIM.