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

Flame Photometry, Lithium

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

JIH is the FDA product code for Flame Photometry, Lithium, a class II device type, regulated under 21 CFR 862.3560. As of , FDA records hold 12 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
JIH
Device name
Flame Photometry, 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
12
Ingested recalls
2

Clearances, product code JIH

By decision year
12 clearances under product code JIH with a decision year between 1977 and 2005, 1977 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code JIH by decision year
YearClearances
19772
19801
19831
19892
19921
19931
19941
20011
20031
20051

Applicants with the most clearances

Product code JIH
Applicants holding the most 510(k) clearances under product code JIH
ApplicantClearances
Eastman Kodak Company2
Abbott Medical1
Akers Biosciences, Inc.1
Akers Laboratories, Inc.1
American Monitor Corp.1
Baxter Healthcare Corporation1
Ciba Corning Diagnostics Corp.1
Corning Medical & Scientific1
Siemens Healthcare Diagnostics Inc.1
Gilford Diagnostics1

Companies listing this code with FDA

Companies whose registered establishments list this code