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

Flame Emission Photometer For Clinical Use

21 CFR 862.2540 / Clinical Chemistry
FDA source (opens on fda.gov)

JJO is the FDA product code for Flame Emission Photometer For Clinical Use, a class I device type, regulated under 21 CFR 862.2540. As of , FDA records hold 22 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
JJO
Device name
Flame Emission Photometer For Clinical Use
Regulation
21 CFR 862.2540
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
22
Ingested recalls
0

Clearances, product code JJO

By decision year
22 clearances under product code JJO with a decision year between 1977 and 1987, 1983 the highest year at 7.
Show the numbers
510(k) clearances under FDA product code JJO by decision year
YearClearances
19772
19782
19791
19821
19837
19846
19851
19861
19871

Applicants with the most clearances

Product code JJO
Applicants holding the most 510(k) clearances under product code JJO
ApplicantClearances
Shaban Mfg. Co.6
Corning Medical & Scientific3
Reagent Laboratory, Inc.3
Instrumentation Laboratory Co.2
Dr. Bruno Lange GmbH1
Finnigan Corp.1
Gilford Instrument Laboratories, Inc.1
Hycel, Inc.1
Logos Scientific, Inc.1
Olympus Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code