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

Flame Photometry, Sodium

21 CFR 862.1665 / Clinical Chemistry
FDA source (opens on fda.gov)

JGT is the FDA product code for Flame Photometry, Sodium, a class II device type, regulated under 21 CFR 862.1665. As of , FDA records hold 8 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JGT
Device name
Flame Photometry, Sodium
Regulation
21 CFR 862.1665
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
8
Ingested recalls
0

Clearances, product code JGT

By decision year
8 clearances under product code JGT with a decision year between 1977 and 1990, 1984 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code JGT by decision year
YearClearances
19771
19801
19811
19843
19891
19901

Applicants with the most clearances

Product code JGT
Applicants holding the most 510(k) clearances under product code JGT
ApplicantClearances
American Monitor Corp.1
Boehringer Mannheim Corp.1
Em Diagnostic Systems, Inc.1
Gilford Diagnostics1
Hi Chem, Inc.1
Sclavo, Inc.1
Shaban Mfg. Co.1
Technicon Instruments Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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