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

Atomic Absorption, Lithium

21 CFR 862.3560 / Clinical Toxicology
FDA source (opens on fda.gov)

JII is the FDA product code for Atomic Absorption, Lithium, a class II device type, regulated under 21 CFR 862.3560. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JII
Device name
Atomic Absorption, Lithium
Regulation
21 CFR 862.3560
Device class
Class II
Review panel
Clinical Toxicology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
3
Ingested recalls
0

Clearances, product code JII

By decision year
3 clearances under product code JII with a decision year between 1991 and 2008, 1991 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code JII by decision year
YearClearances
19911
20031
20081

Applicants with the most clearances

Product code JII
Applicants holding the most 510(k) clearances under product code JII
ApplicantClearances
Diazyme Laboratories, Inc.1
General Atomics1
In Wha Pharmaceutical Co., Ltd.1

Companies listing this code with FDA

Companies whose registered establishments list this code